A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16154991



Internal ID5247608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19092023..19095056hg38UCSC Ensembl
Innerchr20:19092026..19095054hg38UCSC Ensembl
Outerchr20:19092021..19095059hg38UCSC Ensembl
chr20:19072667..19075700hg19UCSC Ensembl
Innerchr20:19072670..19075698hg19UCSC Ensembl
Outerchr20:19072665..19075703hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg383034
hg193034
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645450
Supporting Variants
SamplesNA18633
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16154991
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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