A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691249



Internal ID15081215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90261647..90264628hg38UCSC Ensembl
Innerchr11:89994815..89997796hg19UCSC Ensembl
Innerchr11:89634463..89637444hg18UCSC Ensembl
Innerchr11:89634463..89637444hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg382982
hg192982
hg182982
hg172982
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519936
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691249
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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