A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563007



Internal ID16350416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105580809..105648696hg38UCSC Ensembl
Innerchr13:106233158..106301045hg19UCSC Ensembl
Innerchr13:105031159..105099046hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3867888
hg1967888
hg1867888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3372n54
Supporting Variantsnssv818856, nssv818855, nssv818857
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563007
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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