A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700230



Internal ID15090196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130190322..130199661hg38UCSC Ensembl
Innerchr11:130060217..130069556hg19UCSC Ensembl
Innerchr11:129565427..129574766hg18UCSC Ensembl
Innerchr11:129565427..129574766hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg389340
hg199340
hg189340
hg179340
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517199
Supporting Variants
Samples
Known GenesST14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700230
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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