A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1842n54



Internal ID22769737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54715977..54771612hg38UCSC Ensembl
chr11:51347668..51403303hg19UCSC Ensembl
chr11:51204244..51259879hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3855636
hg1955636
hg1855636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554486, nsv554485
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1842n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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