A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555410



Internal ID15996133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72694823..72720634hg38UCSC Ensembl
Innerchr11:72405868..72431679hg19UCSC Ensembl
Innerchr11:72083516..72109327hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3825812
hg1925812
hg1825812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2006n54
Supporting Variantsnssv1174832
SamplesHGDP01095
Known GenesARAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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