A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702899



Internal ID15439551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114419647..114421292hg38UCSC Ensembl
Innerchr11:114290369..114292014hg19UCSC Ensembl
Innerchr11:113795579..113797224hg18UCSC Ensembl
Innerchr11:113795579..113797224hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg381646
hg191646
hg181646
hg171646
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526581
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702899
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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