A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646132



Internal ID6686191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54027089..54027910hg38UCSC Ensembl
Innerchr20:54027092..54027908hg38UCSC Ensembl
Outerchr20:54027087..54027913hg38UCSC Ensembl
chr20:52643628..52644449hg19UCSC Ensembl
Innerchr20:52643631..52644447hg19UCSC Ensembl
Outerchr20:52643626..52644452hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16206026
SamplesNA19077
Known GenesBCAS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646132
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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