A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553899



Internal ID15994622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26463973..26582379hg38UCSC Ensembl
Innerchr11:26485520..26603926hg19UCSC Ensembl
Innerchr11:26442096..26560502hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38118407
hg19118407
hg18118407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174781
SamplesNINDS_156
Known GenesANO3, MUC15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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