A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645582



Internal ID6685644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25284710..25318462hg38UCSC Ensembl
chr20:25265346..25299098hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3833753
hg1933753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16166456, essv16166457
SamplesHG00629, HG00266
Known GenesABHD12, PYGB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645582
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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