A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561577



Internal ID16348986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:45046636..45081502hg38UCSC Ensembl
Innerchr13:45620771..45655637hg19UCSC Ensembl
Innerchr13:44518771..44553637hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3834867
hg1934867
hg1834867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3134n54
Supporting Variantsnssv810009
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561577
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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