A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555273



Internal ID15995996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67628243..67666398hg38UCSC Ensembl
Innerchr11:67395714..67433869hg19UCSC Ensembl
Innerchr11:67152290..67190445hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3838156
hg1938156
hg1838156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174814
SamplesHGDP00688
Known GenesACY3, ALDH3B2, NUDT8, TBX10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555273
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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