A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700015



Internal ID15089981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60169506..60179779hg38UCSC Ensembl
Innerchr11:59936979..59947252hg19UCSC Ensembl
Innerchr11:59693555..59703828hg18UCSC Ensembl
Innerchr11:59693555..59703828hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3810274
hg1910274
hg1810274
hg1710274
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524137
Supporting Variants
Samples
Known GenesMS4A6A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700015
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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