A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056615



Internal ID19145834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76870692..77008383hg38UCSC Ensembl
Innerchr16:76904589..77042280hg19UCSC Ensembl
Innerchr16:75462090..75599781hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38137692
hg19137692
hg18137692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559656
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)nsv1056615
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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