A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645827



Internal ID7032575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40569099..40573940hg38UCSC Ensembl
Innerchr20:40569099..40573940hg38UCSC Ensembl
Outerchr20:40568987..40574050hg38UCSC Ensembl
chr20:39197739..39202580hg19UCSC Ensembl
Innerchr20:39197739..39202580hg19UCSC Ensembl
Outerchr20:39197627..39202690hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg384842
hg194842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16186588
SamplesHG02429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645827
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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