A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16164057



Internal ID3401125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24904510..24925865hg38UCSC Ensembl
Innerchr20:24904560..24925815hg38UCSC Ensembl
Outerchr20:24904460..24925915hg38UCSC Ensembl
chr20:24885146..24906501hg19UCSC Ensembl
Innerchr20:24885196..24906451hg19UCSC Ensembl
Outerchr20:24885096..24906551hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3821356
hg1921356
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645570
Supporting Variants
SamplesHG03048
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16164057
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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