A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696312



Internal ID15432964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1906987..1917293hg38UCSC Ensembl
Innerchr11:1928217..1938523hg19UCSC Ensembl
Innerchr11:1884793..1895099hg18UCSC Ensembl
Innerchr11:1884793..1895099hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3810307
hg1910307
hg1810307
hg1710307
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518858
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696312
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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