A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562442



Internal ID16349851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81054873..81099338hg38UCSC Ensembl
Innerchr13:81629008..81673473hg19UCSC Ensembl
Innerchr13:80527009..80571474hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3844466
hg1944466
hg1844466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815988
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562442
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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