A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698268



Internal ID15434920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37466130..37471028hg38UCSC Ensembl
Innerchr13:38040267..38045165hg19UCSC Ensembl
Innerchr13:36938267..36943165hg18UCSC Ensembl
Innerchr13:36938267..36943165hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384899
hg194899
hg184899
hg174899
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521650
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698268
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