A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562357



Internal ID16003080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75635847..75636718hg38UCSC Ensembl
Innerchr13:76209983..76210854hg19UCSC Ensembl
Innerchr13:75107984..75108855hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38872
hg19872
hg18872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3259n54
Supporting Variantsnssv815778
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562357
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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