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nsv6625625

  • Variant Calls:31
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43,417

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1093 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):1,452,367-1,495,783Question Mark
Overlapping variant regions from other studies: 1093 SVs from 78 studies. See in: genome view    
Submitted genomic1,387,747-1,431,163Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6625625RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr11,452,3671,495,783
nsv6625625Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr11,387,7471,431,163

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18281832deletionOSC2188SNP arrayProbe signal intensity8
nssv18282597deletionOSC2062SNP arrayProbe signal intensity6
nssv18282810deletionOSC2225SNP arrayProbe signal intensitynssv18282811, nssv18282189
nssv18284243deletionOSC2580SNP arrayProbe signal intensitynssv18285182, nssv18285183, nssv18285184
nssv18284670deletionOSC2717SNP arrayProbe signal intensity6
nssv18287071deletionOSC3105SNP arrayProbe signal intensity5
nssv18287668deletionOSC3056SNP arrayProbe signal intensity11
nssv18287921deletionOSC3199SNP arrayProbe signal intensity5
nssv18287999deletionOSC3253SNP arrayProbe signal intensity6
nssv18288042deletionOSC3283SNP arrayProbe signal intensitynssv18288272, nssv18288607, nssv18288907
nssv18288661deletionOSC3317SNP arrayProbe signal intensity8
nssv18290298deletionOSC3584SNP arrayProbe signal intensity8
nssv18290818deletionOSC0392SNP arrayProbe signal intensity7
nssv18291252deletionOSC3637SNP arrayProbe signal intensity7
nssv18292059deletionOSC4013SNP arrayProbe signal intensitynssv18292058, nssv18292753, nssv18293335
nssv18292329deletionOSC3957SNP arrayProbe signal intensity5
nssv18295673deletionOSC4619SNP arrayProbe signal intensitynssv18295674, nssv18295447
nssv18300034deletionOSC0546SNP arrayProbe signal intensity9
nssv18311631deletionOSC0776SNP arrayProbe signal intensity5
nssv18313348deletionOSC0798SNP arrayProbe signal intensitynssv18313347, nssv18313352, nssv18313356
nssv18315345deletionOSC0841SNP arrayProbe signal intensity9
nssv18321213deletionOSC1224SNP arrayProbe signal intensity11
nssv18322670deletionOSC1345SNP arrayProbe signal intensitynssv18323211
nssv18322878deletionOSC1493SNP arrayProbe signal intensity10
nssv18323212deletionOSC1346SNP arrayProbe signal intensity13
nssv18323295deletionOSC1399SNP arrayProbe signal intensitynssv18323296
nssv18323898deletionOSC1572SNP arrayProbe signal intensity7
nssv18324419deletionOSC1739SNP arrayProbe signal intensitynssv18323765, nssv18325061, nssv18323766
nssv18324780deletionOSC1805SNP arrayProbe signal intensity8
nssv18325109deletionOSC1774SNP arrayProbe signal intensitynssv18323812, nssv18325397, nssv18323811
nssv18325299deletionOSC1906SNP arrayProbe signal intensity11

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18281832RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18282597RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18282810RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18284243RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18284670RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18287071RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18287668RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18287921RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18287999RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18288042RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18288661RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18290298RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18290818RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18291252RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18292059RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18292329RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18295673RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18300034RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18311631RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18313348RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18315345RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18321213RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18322670RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18322878RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18323212RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18323295RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18323898RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18324419RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18324780RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18325109RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18325299RemappedPerfectNC_000001.11:g.(?_
1452367)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,452,3671,495,783
nssv18281832Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18282597Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18282810Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18284243Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18284670Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18287071Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18287668Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18287921Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18287999Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18288042Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18288661Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18290298Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18290818Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18291252Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18292059Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18292329Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18295673Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18300034Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18311631Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18313348Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18315345Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18321213Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18322670Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18322878Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18323212Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18323295Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18323898Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18324419Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18324780Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18325109Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163
nssv18325299Submitted genomicNC_000001.10:g.(?_
1387747)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,387,7471,431,163

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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