A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684438



Internal ID15421090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64038696..64073143hg38UCSC Ensembl
Innerchr16:64072600..64107047hg19UCSC Ensembl
Innerchr16:62630101..62664548hg18UCSC Ensembl
Innerchr16:62630101..62664548hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3834448
hg1934448
hg1834448
hg1734448
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516354
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684438
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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