A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702178



Internal ID15438830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90818316..90823189hg38UCSC Ensembl
Innerchr11:90551484..90556357hg19UCSC Ensembl
Innerchr11:90191132..90196005hg18UCSC Ensembl
Innerchr11:90191132..90196005hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384874
hg194874
hg184874
hg174874
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521151
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702178
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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