A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526408



Internal ID15107015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44188733..44195887hg38UCSC Ensembl
Innerchr6:44156470..44163624hg19UCSC Ensembl
Innerchr6:44264448..44271602hg18UCSC Ensembl
Innerchr6:44264448..44271602hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg387155
hg197155
hg187155
hg177155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702708
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526408
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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