A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4669n54



Internal ID22772564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77818881..77820182hg38UCSC Ensembl
chr15:78111223..78112524hg19UCSC Ensembl
chr15:75898278..75899579hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg381302
hg191302
hg181302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570176, nsv570191, nsv570178, nsv570183, nsv570186, nsv570189, nsv570188
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4669n54
Frequency
Sample Size17421
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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