A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517743



Internal ID15098350
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653078, nssv660558, nssv674145
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517743
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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