A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174832



Internal ID15531414
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 StatusS
Merged Variantsnsv555410
Supporting Variants
SamplesHGDP01095
Known GenesARAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174832
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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