A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052516



Internal ID19141735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73078626..73101853hg38UCSC Ensembl
Innerchr13:73652764..73675991hg19UCSC Ensembl
Innerchr13:72550765..72573992hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3823228
hg1923228
hg1823228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530504
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)nsv1052516
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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