A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646898



Internal ID7033640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32837966..32852486hg38UCSC Ensembl
Innerchr21:32838466..32851985hg38UCSC Ensembl
Outerchr21:32836966..32853486hg38UCSC Ensembl
chr21:34210276..34224795hg19UCSC Ensembl
Innerchr21:34210776..34224295hg19UCSC Ensembl
Outerchr21:34209276..34225795hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3814521
hg1914520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16313553
SamplesNA19788
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646898
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