A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692888



Internal ID15082854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130168592..130206439hg38UCSC Ensembl
Innerchr11:130038487..130076334hg19UCSC Ensembl
Innerchr11:129543697..129581544hg18UCSC Ensembl
Innerchr11:129543697..129581544hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3837848
hg1937848
hg1837848
hg1737848
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517199
Supporting Variants
Samples
Known GenesST14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692888
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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