A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15292777



Internal ID5294593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74020554..74056594hg38UCSC Ensembl
chr15:74312895..74348935hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3836041
hg1936041
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636900
Supporting Variants
SamplesNA12813
Known GenesPML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15292777
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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