A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686858



Internal ID15423510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479860..134514686hg38UCSC Ensembl
Innerchr11:134349754..134384580hg19UCSC Ensembl
Innerchr11:133854964..133889790hg18UCSC Ensembl
Innerchr11:133854964..133889790hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3834827
hg1934827
hg1834827
hg1734827
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686858
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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