A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519812



Internal ID15100419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52605106..52611885hg38UCSC Ensembl
Innerchr6:52469904..52476683hg19UCSC Ensembl
Innerchr6:52577863..52584642hg18UCSC Ensembl
Innerchr6:52577863..52584642hg17UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg386780
hg196780
hg186780
hg176780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697064
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519812
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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