A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562638



Internal ID16350047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88859658..88912396hg38UCSC Ensembl
Innerchr13:89511912..89564650hg19UCSC Ensembl
Innerchr13:88309913..88362651hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3852739
hg1952739
hg1852739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3302n54
Supporting Variantsnssv816816
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer