A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563163



Internal ID16350572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110933951..110951541hg38UCSC Ensembl
Innerchr13:111586298..111603888hg19UCSC Ensembl
Innerchr13:110384299..110401889hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3817591
hg1917591
hg1817591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819920
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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