A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036901



Internal ID19126120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80936492..81418954hg38UCSC Ensembl
Innerchr13:81510627..81993089hg19UCSC Ensembl
Innerchr13:80408628..80891090hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38482463
hg19482463
hg18482463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713242
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)nsv1036901
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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