A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523437



Internal ID15104044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84176132..84196770hg38UCSC Ensembl
Innerchr16:84209738..84230376hg19UCSC Ensembl
Innerchr16:82767239..82787877hg18UCSC Ensembl
Innerchr16:82767239..82787877hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3820639
hg1920639
hg1820639
hg1720639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699193
Samples
Known GenesADAD2, DNAAF1, TAF1C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523437
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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