A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645047



Internal ID6685110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3734083..3737371hg38UCSC Ensembl
Innerchr20:3734104..3737351hg38UCSC Ensembl
Outerchr20:3734063..3737392hg38UCSC Ensembl
chr20:3714730..3718018hg19UCSC Ensembl
Innerchr20:3714751..3717998hg19UCSC Ensembl
Outerchr20:3714710..3718039hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383289
hg193289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16121948
SamplesHG01936
Known GenesHSPA12B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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