A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553895



Internal ID16341304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25751775..25903262hg38UCSC Ensembl
Innerchr11:25773322..25924809hg19UCSC Ensembl
Innerchr11:25729898..25881385hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38151488
hg19151488
hg18151488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174777
SamplesHGDP00869
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553895
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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