A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16163037



Internal ID6461293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23128763..23129886hg38UCSC Ensembl
Innerchr20:23128796..23129854hg38UCSC Ensembl
Outerchr20:23128731..23129919hg38UCSC Ensembl
chr20:23109400..23110523hg19UCSC Ensembl
Innerchr20:23109433..23110491hg19UCSC Ensembl
Outerchr20:23109368..23110556hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645518
Supporting Variants
SamplesNA20516
Known GenesLINC00656
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16163037
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