A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527957



Internal ID15108564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84389209..84394686hg38UCSC Ensembl
Innerchr16:84422815..84428292hg19UCSC Ensembl
Innerchr16:82980316..82985793hg18UCSC Ensembl
Innerchr16:82980316..82985793hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385478
hg195478
hg185478
hg175478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704467
Samples
Known GenesATP2C2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527957
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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