A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698640



Internal ID15088606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38843280..38886797hg38UCSC Ensembl
Innerchr11:38864830..38908347hg19UCSC Ensembl
Innerchr11:38821406..38864923hg18UCSC Ensembl
Innerchr11:38821406..38864923hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3843518
hg1943518
hg1843518
hg1743518
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522970
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698640
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