A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053839



Internal ID18796370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:33050208..33072917hg38UCSC Ensembl
Innerchr13:33624345..33647054hg19UCSC Ensembl
Innerchr13:32522345..32545054hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3822710
hg1922710
hg1822710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523238
Samples
Known GenesKL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053839
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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