A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518890



Internal ID15446183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23947346..23955427hg38UCSC Ensembl
Innerchr13:24521485..24529566hg19UCSC Ensembl
Innerchr13:23419485..23427566hg18UCSC Ensembl
Innerchr13:23419485..23427566hg17UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg388082
hg198082
hg188082
hg178082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696348
Samples
Known GenesANKRD20A19P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518890
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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