A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694162



Internal ID15430814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64049047..64073143hg38UCSC Ensembl
Innerchr16:64082951..64107047hg19UCSC Ensembl
Innerchr16:62640452..62664548hg18UCSC Ensembl
Innerchr16:62640452..62664548hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3824097
hg1924097
hg1824097
hg1724097
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)nssv694162
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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