A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699216



Internal ID15089182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52439351..52468212hg38UCSC Ensembl
Innerchr16:52473263..52502124hg19UCSC Ensembl
Innerchr16:51030764..51059625hg18UCSC Ensembl
Innerchr16:51030764..51059625hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3828862
hg1928862
hg1828862
hg1728862
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523458
Supporting Variants
Samples
Known GenesTOX3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699216
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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