A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4556n54



Internal ID22772451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57330402..57498238hg38UCSC Ensembl
chr15:57622600..57790436hg19UCSC Ensembl
chr15:55409892..55577728hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38167837
hg19167837
hg18167837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569586, nsv569582, nsv569581, nsv569579, nsv569583, nsv569587, nsv569580, nsv569589, nsv569585, nsv569588, nsv569584
Samples1782681495_A
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4556n54
Frequency
Sample Size17421
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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