A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601681



Internal ID16389090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31315520..31349322hg38UCSC Ensembl
Innerchr6:31283297..31317099hg19UCSC Ensembl
Innerchr6:31391276..31425078hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3833803
hg1933803
hg1833803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10381n54
Supporting Variantsnssv1053045, nssv1053044, nssv1053047, nssv1053046
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601681
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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