A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2006n54



Internal ID20135430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72694178..72730386hg38UCSC Ensembl
chr11:72405223..72441431hg19UCSC Ensembl
chr11:72082871..72119079hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3836209
hg1936209
hg1836209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555410, nsv555408
SamplesHGDP01095
Known GenesARAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2006n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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