A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561703



Internal ID16349112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54569619..54899597hg38UCSC Ensembl
Innerchr13:55143754..55473732hg19UCSC Ensembl
Innerchr13:54041755..54371733hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38329979
hg19329979
hg18329979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811791, nssv811792
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561703
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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