A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16163971



Internal ID3889494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24670892..24841772hg38UCSC Ensembl
chr20:24651528..24822408hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38170881
hg19170881
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645556
Supporting Variants
SamplesHG03539
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16163971
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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