A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561187



Internal ID16001910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18877750..19084941hg38UCSC Ensembl
Innerchr13:19451890..19659081hg19UCSC Ensembl
Innerchr13:18349890..18557081hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38207192
hg19207192
hg18207192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806024
Samples
Known GenesLINC00408, LINC00442
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561187
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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