A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556037



Internal ID16343446
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 StatusM
Merged Variants
Supporting Variantsnssv781712, nssv1174921
SamplesNINDS_183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556037
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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