A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701458



Internal ID15438110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55054313..55059506hg38UCSC Ensembl
Innerchr16:55088225..55093418hg19UCSC Ensembl
Innerchr16:53645726..53650919hg18UCSC Ensembl
Innerchr16:53645726..53650919hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg385194
hg195194
hg185194
hg175194
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525340
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701458
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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