A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645705



Internal ID7032454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34694793..34695660hg38UCSC Ensembl
Innerchr20:34694820..34695633hg38UCSC Ensembl
Outerchr20:34694766..34695687hg38UCSC Ensembl
chr20:33282597..33283464hg19UCSC Ensembl
Innerchr20:33282624..33283437hg19UCSC Ensembl
Outerchr20:33282570..33283491hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16178325, essv16178329, essv16178323, essv16178326, essv16178322, essv16178332, essv16178321, essv16178333, essv16178324, essv16178331, essv16178327, essv16178328, essv16178330
SamplesHG03965, NA21115, HG04164, HG03978, HG03861, HG04189, HG02725, HG04227, HG04239, NA21123, HG03850, HG03702, HG03922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645705
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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