A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669555



Internal ID15406207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74709838..74767412hg38UCSC Ensembl
Innerchr16:74743736..74801310hg19UCSC Ensembl
Innerchr16:73301237..73358811hg18UCSC Ensembl
Innerchr16:73301237..73358811hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3857575
hg1957575
hg1857575
hg1757575
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)nssv669555
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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