A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637119



Internal ID7023913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85554098..85633998hg38UCSC Ensembl
chr15:86097329..86177229hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3879901
hg1979901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15315490
SamplesNA19043
Known GenesAKAP13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637119
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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