A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699182



Internal ID15435834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:50839084..50843477hg38UCSC Ensembl
Innerchr16:50872995..50877388hg19UCSC Ensembl
Innerchr16:49430496..49434889hg18UCSC Ensembl
Innerchr16:49430496..49434889hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg384394
hg194394
hg184394
hg174394
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523427
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699182
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer