A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562361



Internal ID16003084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75636175..75636921hg38UCSC Ensembl
Innerchr13:76210311..76211057hg19UCSC Ensembl
Innerchr13:75108312..75109058hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38747
hg19747
hg18747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3260n54
Supporting Variantsnssv815782, nssv815783
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562361
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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