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nsv6625378

  • Variant Calls:31
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,075

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1100 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):1,450,709-1,495,783Question Mark
Overlapping variant regions from other studies: 1100 SVs from 78 studies. See in: genome view    
Submitted genomic1,386,089-1,431,163Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6625378RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr11,450,7091,495,783
nsv6625378Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr11,386,0891,431,163

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18282864deletionOSC2268SNP arrayProbe signal intensity7
nssv18283299deletionOSC2369SNP arrayProbe signal intensity5
nssv18284777deletionOSC2528SNP arrayProbe signal intensity7
nssv18285127deletionOSC2547SNP arrayProbe signal intensity9
nssv18285568deletionOSC0029SNP arrayProbe signal intensitynssv18286179, nssv18286454
nssv18286506deletionOSC2878SNP arrayProbe signal intensity10
nssv18287359duplicationOSC0315SNP arrayProbe signal intensity6
nssv18287595deletionOSC3003SNP arrayProbe signal intensity7
nssv18287601deletionOSC3008SNP arrayProbe signal intensitynssv18286699, nssv18286700, nssv18287600
nssv18288586deletionOSC3271SNP arrayProbe signal intensity10
nssv18289100deletionOSC3391SNP arrayProbe signal intensity10
nssv18289443deletionOSC3460SNP arrayProbe signal intensitynssv18289769, nssv18289200, nssv18289444
nssv18289906deletionOSC3557SNP arrayProbe signal intensity5
nssv18290181deletionOSC3535SNP arrayProbe signal intensity13
nssv18291017deletionOSC3680SNP arrayProbe signal intensitynssv18290686, nssv18290427
nssv18291454deletionOSC3769SNP arrayProbe signal intensitynssv18291453, nssv18291142, nssv18290547
nssv18291630deletionOSC3882SNP arrayProbe signal intensity8
nssv18292769deletionOSC4026SNP arrayProbe signal intensity13
nssv18292790deletionOSC4040SNP arrayProbe signal intensity6
nssv18292911deletionOSC4118SNP arrayProbe signal intensity9
nssv18293127deletionOSC4114SNP arrayProbe signal intensitynssv18293483, nssv18293128, nssv18293126
nssv18294246deletionOSC4428SNP arrayProbe signal intensity5
nssv18294437deletionOSC4386SNP arrayProbe signal intensity7
nssv18296856deletionOSC4808SNP arrayProbe signal intensitynssv18296620, nssv18296857
nssv18297122deletionOSC4767SNP arrayProbe signal intensity6
nssv18300695deletionOSC5615SNP arrayProbe signal intensity6
nssv18306839deletionOSC0698SNP arrayProbe signal intensity7
nssv18320596deletionOSC0990SNP arrayProbe signal intensity7
nssv18320882deletionOSC0991SNP arrayProbe signal intensity7
nssv18320909deletionOSC1009SNP arrayProbe signal intensity5
nssv18324169deletionOSC0161SNP arrayProbe signal intensitynssv18323531, nssv18324456

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18282864RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18283299RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18284777RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18285127RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18285568RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18286506RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18287359RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)dup
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18287595RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18287601RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18288586RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18289100RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18289443RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18289906RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18290181RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18291017RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18291454RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18291630RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18292769RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18292790RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18292911RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18293127RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18294246RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18294437RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18296856RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18297122RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18300695RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18306839RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18320596RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18320882RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18320909RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18324169RemappedPerfectNC_000001.11:g.(?_
1450709)_(1495783_
?)del
GRCh38.p12First PassNC_000001.11Chr11,450,7091,495,783
nssv18282864Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18283299Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18284777Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18285127Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18285568Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18286506Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18287359Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)dup
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18287595Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18287601Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18288586Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18289100Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18289443Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18289906Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18290181Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18291017Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18291454Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18291630Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18292769Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18292790Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18292911Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18293127Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18294246Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18294437Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18296856Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18297122Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18300695Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18306839Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18320596Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18320882Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18320909Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163
nssv18324169Submitted genomicNC_000001.10:g.(?_
1386089)_(1431163_
?)del
GRCh37 (hg19)NC_000001.10Chr11,386,0891,431,163

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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