A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637182



Internal ID6677289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89038688..89124261hg38UCSC Ensembl
chr15:89581919..89667492hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3885574
hg1985574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317058
SamplesHG03479
Known GenesABHD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637182
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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