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nsv6620317

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:735,413

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1611 SVs from 73 studies. See in: genome view    
Remapped(Score: Perfect):117,664,956-118,400,368Question Mark
Overlapping variant regions from other studies: 1612 SVs from 73 studies. See in: genome view    
Submitted genomic119,424,467-120,159,880Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6620317RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10117,664,956118,400,368
nsv6620317Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10119,424,467120,159,880

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18310934duplicationOSC7189SNP arrayProbe signal intensity10

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18310934RemappedPerfectNC_000010.11:g.(?_
117664956)_(118400
368_?)dup
GRCh38.p12First PassNC_000010.11Chr10117,664,956118,400,368
nssv18310934Submitted genomicNC_000010.10:g.(?_
119424467)_(120159
880_?)dup
GRCh37 (hg19)NC_000010.10Chr10119,424,467120,159,880

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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