A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174821



Internal ID15876663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69595537..69615426hg38UCSC Ensembl
Innerchr11:69410305..69430194hg19UCSC Ensembl
Innerchr11:69119486..69139375hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3819890
hg1919890
hg1819890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555323
Supporting Variants
SamplesHGDP00878
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174821
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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