A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701306



Internal ID15091272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2868291..2869928hg38UCSC Ensembl
Innerchr16:2918292..2919929hg19UCSC Ensembl
Innerchr16:2858293..2859930hg18UCSC Ensembl
Innerchr16:2858293..2859930hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381638
hg191638
hg181638
hg171638
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525220
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701306
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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