A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688261



Internal ID15078227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5254021..5301110hg38UCSC Ensembl
Innerchr16:5304022..5351111hg19UCSC Ensembl
Innerchr16:5244023..5291112hg18UCSC Ensembl
Innerchr16:5244023..5291112hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3847090
hg1947090
hg1847090
hg1747090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516117
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688261
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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