A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696370



Internal ID15433022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74712899..74719181hg38UCSC Ensembl
Innerchr16:74746797..74753079hg19UCSC Ensembl
Innerchr16:73304298..73310580hg18UCSC Ensembl
Innerchr16:73304298..73310580hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg386283
hg196283
hg186283
hg176283
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517513
Supporting Variants
Samples
Known GenesFA2H
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696370
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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