A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563379



Internal ID16350788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113452383..113477639hg38UCSC Ensembl
Innerchr13:114106698..114131954hg19UCSC Ensembl
Innerchr13:113154699..113179955hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3825257
hg1925257
hg1825257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149462
Samples1780862304_A
Known GenesADPRHL1, DCUN1D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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