A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561701



Internal ID16349110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54137141..54251969hg38UCSC Ensembl
Innerchr13:54711276..54826104hg19UCSC Ensembl
Innerchr13:53609277..53724105hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38114829
hg19114829
hg18114829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811789
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561701
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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