A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563022



Internal ID16350431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108078533..108102568hg38UCSC Ensembl
Innerchr13:108730881..108754916hg19UCSC Ensembl
Innerchr13:107528882..107552917hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3824036
hg1924036
hg1824036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3377n54
Supporting Variantsnssv819258
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563022
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