A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562161



Internal ID16349570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68666813..68698025hg38UCSC Ensembl
Innerchr13:69240945..69272157hg19UCSC Ensembl
Innerchr13:68138946..68170158hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3831213
hg1931213
hg1831213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3226n54
Supporting Variantsnssv813450, nssv813451
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562161
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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