A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701103



Internal ID15437755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117959714..117961094hg38UCSC Ensembl
Innerchr11:117830429..117831809hg19UCSC Ensembl
Innerchr11:117335639..117337019hg18UCSC Ensembl
Innerchr11:117335639..117337019hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381381
hg191381
hg181381
hg171381
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525055
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701103
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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