A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174921



Internal ID15880264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98683202..98724905hg38UCSC Ensembl
Innerchr11:98553932..98595635hg19UCSC Ensembl
Innerchr11:98059142..98100845hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3841704
hg1941704
hg1841704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556037
Supporting Variants
SamplesNINDS_183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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