A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698949



Internal ID15088915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84397270..84455427hg38UCSC Ensembl
Innerchr16:84430876..84489033hg19UCSC Ensembl
Innerchr16:82988377..83046534hg18UCSC Ensembl
Innerchr16:82988377..83046534hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3858158
hg1958158
hg1858158
hg1758158
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523226
Supporting Variants
Samples
Known GenesATP2C2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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