A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063797



Internal ID19153016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:50393643..50421816hg38UCSC Ensembl
Innerchr16:50427554..50455727hg19UCSC Ensembl
Innerchr16:48985055..49013228hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3828174
hg1928174
hg1828174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722705
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)nsv1063797
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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