A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694227



Internal ID15084193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84194593..84196629hg38UCSC Ensembl
Innerchr16:84228199..84230235hg19UCSC Ensembl
Innerchr16:82785700..82787736hg18UCSC Ensembl
Innerchr16:82785700..82787736hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382037
hg192037
hg182037
hg172037
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518342
Supporting Variants
Samples
Known GenesADAD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694227
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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