A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555238



Internal ID15995961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66945101..66945634hg38UCSC Ensembl
Innerchr11:66712572..66713105hg19UCSC Ensembl
Innerchr11:66469148..66469681hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38534
hg19534
hg18534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778546, nssv778547
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555238
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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