A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525542



Internal ID18477137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103283608..103487558hg38UCSC Ensembl
Innerchr13:103935958..104139908hg19UCSC Ensembl
Innerchr13:102733959..102937909hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38203951
hg19203951
hg18203951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052575
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)nssv3525542
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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