A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065438



Internal ID19154657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58344491..58387191hg38UCSC Ensembl
Innerchr16:58378395..58421095hg19UCSC Ensembl
Innerchr16:56935896..56978596hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3842701
hg1942701
hg1842701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2990n100
Supporting Variantsnssv3722716
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)nsv1065438
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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