A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562349



Internal ID16003072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75635643..75636503hg38UCSC Ensembl
Innerchr13:76209779..76210639hg19UCSC Ensembl
Innerchr13:75107780..75108640hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38861
hg19861
hg18861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3257n54
Supporting Variantsnssv815768
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562349
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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