A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042359



Internal ID19131578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105016508..105093401hg38UCSC Ensembl
Innerchr13:105668859..105745752hg19UCSC Ensembl
Innerchr13:104466860..104543753hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3876894
hg1976894
hg1876894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525556
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)nsv1042359
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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