A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667941



Internal ID15404593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74712899..74752203hg38UCSC Ensembl
Innerchr16:74746797..74786101hg19UCSC Ensembl
Innerchr16:73304298..73343602hg18UCSC Ensembl
Innerchr16:73304298..73343602hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3839305
hg1939305
hg1839305
hg1739305
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)nssv667941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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