A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645791



Internal ID6685852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38858020..38867590hg38UCSC Ensembl
Innerchr20:38858020..38867590hg38UCSC Ensembl
Outerchr20:38857903..38867734hg38UCSC Ensembl
chr20:37486663..37496233hg19UCSC Ensembl
Innerchr20:37486663..37496233hg19UCSC Ensembl
Outerchr20:37486546..37496377hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389571
hg199571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16182080
SamplesHG02131
Known GenesPPP1R16B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645791
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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