A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562347



Internal ID16003070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75558104..75579279hg38UCSC Ensembl
Innerchr13:76132240..76153415hg19UCSC Ensembl
Innerchr13:75030241..75051416hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3821176
hg1921176
hg1821176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815765
Samples
Known GenesUCHL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562347
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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