A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655688



Internal ID15045654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70690022..70741552hg38UCSC Ensembl
Innerchr16:70723925..70775455hg19UCSC Ensembl
Innerchr16:69281426..69332956hg18UCSC Ensembl
Innerchr16:69281426..69332956hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3851531
hg1951531
hg1851531
hg1751531
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesVAC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655688
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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