A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16163913



Internal ID3810979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24253259..24256026hg38UCSC Ensembl
Innerchr20:24253272..24256013hg38UCSC Ensembl
Outerchr20:24253246..24256039hg38UCSC Ensembl
chr20:24233895..24236662hg19UCSC Ensembl
Innerchr20:24233908..24236649hg19UCSC Ensembl
Outerchr20:24233882..24236675hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382768
hg192768
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645545
Supporting Variants
SamplesHG03452
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16163913
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer