A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522608



Internal ID15449901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2032025..2203654hg38UCSC Ensembl
Innerchr6:2032259..2203888hg19UCSC Ensembl
Innerchr6:1977258..2148887hg18UCSC Ensembl
Innerchr6:1977258..2148887hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38171630
hg19171630
hg18171630
hg17171630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706000
Samples
Known GenesGMDS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522608
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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