A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1718n54



Internal ID22769613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25528784..25563561hg38UCSC Ensembl
chr11:25550330..25585107hg19UCSC Ensembl
chr11:25506906..25541683hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3834778
hg1934778
hg1834778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553868, nsv553869
SamplesNINDS_125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1718n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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