A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686619



Internal ID15076585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5235393..5299134hg38UCSC Ensembl
Innerchr16:5285394..5349135hg19UCSC Ensembl
Innerchr16:5225395..5289136hg18UCSC Ensembl
Innerchr16:5225395..5289136hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3863742
hg1963742
hg1863742
hg1763742
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)nssv686619
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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