A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694484



Internal ID15431136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104367589..104369870hg38UCSC Ensembl
Innerchr13:105019939..105022220hg19UCSC Ensembl
Innerchr13:103817940..103820221hg18UCSC Ensembl
Innerchr13:103817940..103820221hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg382282
hg192282
hg182282
hg172282
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521724
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694484
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