A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523736



Internal ID15104343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69319684..69321770hg38UCSC Ensembl
Innerchr16:69353587..69355673hg19UCSC Ensembl
Innerchr16:67911088..67913174hg18UCSC Ensembl
Innerchr16:67911088..67913174hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382087
hg192087
hg182087
hg172087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699552
Samples
Known GenesVPS4A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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