A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516474



Internal ID15443767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7806210..7807799hg38UCSC Ensembl
Innerchr16:7856212..7857801hg19UCSC Ensembl
Innerchr16:7796213..7797802hg18UCSC Ensembl
Innerchr16:7796213..7797802hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381590
hg191590
hg181590
hg171590
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700192, nssv676987, nssv668588
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516474
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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