A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815777



Internal ID15763047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75635847..75636554hg38UCSC Ensembl
Innerchr13:76209983..76210690hg19UCSC Ensembl
Innerchr13:75107984..75108691hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38708
hg19708
hg18708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562356
Supporting Variants
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv815777
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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