A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562359



Internal ID16003082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75636005..75636718hg38UCSC Ensembl
Innerchr13:76210141..76210854hg19UCSC Ensembl
Innerchr13:75108142..75108855hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38714
hg19714
hg18714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815780
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562359
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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