A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067267



Internal ID19156486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65420856..65539932hg38UCSC Ensembl
Innerchr16:65454759..65573835hg19UCSC Ensembl
Innerchr16:64012260..64131336hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38119077
hg19119077
hg18119077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2995n100
Supporting Variantsnssv3559439
Samples
Known GenesLINC00922
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067267
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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