A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555324



Internal ID16342733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69599509..69616648hg38UCSC Ensembl
Innerchr11:69414277..69431416hg19UCSC Ensembl
Innerchr11:69123458..69140597hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3817140
hg1917140
hg1817140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1991n54
Supporting Variantsnssv1174822
SamplesHGDP01017
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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