A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521151



Internal ID15448444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90736650..90861031hg38UCSC Ensembl
Innerchr11:90469818..90594199hg19UCSC Ensembl
Innerchr11:90109466..90233847hg18UCSC Ensembl
Innerchr11:90109466..90233847hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38124382
hg19124382
hg18124382
hg17124382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693510, nssv683100, nssv702178
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521151
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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