A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516216



Internal ID15443509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44732193..44734889hg38UCSC Ensembl
Innerchr13:45306329..45309025hg19UCSC Ensembl
Innerchr13:44204329..44207025hg18UCSC Ensembl
Innerchr13:44204329..44207025hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg382697
hg192697
hg182697
hg172697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666870, nssv659414
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516216
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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