A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053627



Internal ID19142846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63392585..63415923hg38UCSC Ensembl
Innerchr11:63160057..63183395hg19UCSC Ensembl
Innerchr11:62916633..62939971hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3823339
hg1923339
hg1823339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520078
Samples
Known GenesMIR3680-1, MIR3680-2, SLC22A9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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