A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523139



Internal ID18821420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21905551..21934115hg38UCSC Ensembl
Innerchr13:22479690..22508254hg19UCSC Ensembl
Innerchr13:21377690..21406254hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3828565
hg1928565
hg1828565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036087
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)nssv3523139
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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