A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175397



Internal ID15874991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106527293..106528755hg38UCSC Ensembl
Innerchr11:106398020..106399482hg19UCSC Ensembl
Innerchr11:105903230..105904692hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381463
hg191463
hg181463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556226
Supporting Variants
SamplesHGDP00618
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175397
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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