A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561699



Internal ID16349108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53859055..53909118hg38UCSC Ensembl
Innerchr13:54433190..54483253hg19UCSC Ensembl
Innerchr13:53331191..53381254hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3850064
hg1950064
hg1850064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811788
Samples
Known GenesLINC00558
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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