A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11744n54



Internal ID22779639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155260564..155288839hg38UCSC Ensembl
chr7:155052274..155080549hg19UCSC Ensembl
chr7:154683207..154711482hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3828276
hg1928276
hg1828276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609122, nsv609123
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11744n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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