A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561464



Internal ID16348873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34982880..34990559hg38UCSC Ensembl
Innerchr13:35557017..35564696hg19UCSC Ensembl
Innerchr13:34455017..34462696hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg387680
hg197680
hg187680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807651, nssv807650
Samples
Known GenesNBEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561464
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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