A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561387



Internal ID16348796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27466918..27495716hg38UCSC Ensembl
Innerchr13:28041055..28069853hg19UCSC Ensembl
Innerchr13:26939055..26967853hg18UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3828799
hg1928799
hg1828799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807239
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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