A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563122



Internal ID16350531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110568495..110608920hg38UCSC Ensembl
Innerchr13:111220842..111261267hg19UCSC Ensembl
Innerchr13:110018843..110059268hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3840426
hg1940426
hg1840426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819757
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563122
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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