A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553775



Internal ID16341184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23980429..24302026hg38UCSC Ensembl
Innerchr11:24001975..24323572hg19UCSC Ensembl
Innerchr11:23958551..24280148hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38321598
hg19321598
hg18321598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174754
SamplesHGDP00705
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553775
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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