A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674145



Internal ID15064111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70030086..70102302hg38UCSC Ensembl
Innerchr16:70063989..70136205hg19UCSC Ensembl
Innerchr16:68621490..68693706hg18UCSC Ensembl
Innerchr16:68621490..68693706hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3872217
hg1972217
hg1872217
hg1772217
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517743
Supporting Variants
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674145
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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