A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701296



Internal ID15437948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126171309..126190188hg38UCSC Ensembl
Innerchr11:126041204..126060083hg19UCSC Ensembl
Innerchr11:125546414..125565293hg18UCSC Ensembl
Innerchr11:125546414..125565293hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3818880
hg1918880
hg1818880
hg1718880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525213
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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