A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656947



Internal ID15393599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:364930..376432hg38UCSC Ensembl
Innerchr16:414930..426432hg19UCSC Ensembl
Innerchr16:354931..366433hg18UCSC Ensembl
Innerchr16:354931..366433hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3811503
hg1911503
hg1811503
hg1711503
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517471
Supporting Variants
Samples
Known GenesMRPL28, TMEM8A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656947
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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