A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563304



Internal ID16350713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113207659..113211022hg38UCSC Ensembl
Innerchr13:113861973..113865336hg19UCSC Ensembl
Innerchr13:112909974..112913337hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383364
hg193364
hg183364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3435n54
Supporting Variantsnssv820490
Samples
Known GenesCUL4A, PCID2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563304
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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