A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525516



Internal ID18477111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97119353..97150042hg38UCSC Ensembl
Innerchr13:97771607..97802296hg19UCSC Ensembl
Innerchr13:96569608..96600297hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3830690
hg1930690
hg1830690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053686
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)nssv3525516
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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