A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555173



Internal ID15995896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62372597..62415535hg38UCSC Ensembl
Innerchr11:62140069..62183007hg19UCSC Ensembl
Innerchr11:61896645..61939583hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3842939
hg1942939
hg1842939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174805
SamplesNINDS_271
Known GenesASRGL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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