A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561592



Internal ID16349001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48957415..48961178hg38UCSC Ensembl
Innerchr13:49531551..49535314hg19UCSC Ensembl
Innerchr13:48429552..48433315hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg383764
hg193764
hg183764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv810018
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561592
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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