A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663232



Internal ID15053198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124985266..125065461hg38UCSC Ensembl
Innerchr11:124855162..124935357hg19UCSC Ensembl
Innerchr11:124360372..124440567hg18UCSC Ensembl
Innerchr11:124360372..124440567hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3880196
hg1980196
hg1880196
hg1780196
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520010
Supporting Variants
Samples
Known GenesCCDC15, SLC37A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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