A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719076



Internal ID19017357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80175470..80213153hg38UCSC Ensembl
Innerchr16:80209367..80247050hg19UCSC Ensembl
Innerchr16:78766868..78804551hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3837684
hg1937684
hg1837684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3719076
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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