A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646538



Internal ID7033282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19941402..20061577hg38UCSC Ensembl
Innerchr21:19941552..20061427hg38UCSC Ensembl
Outerchr21:19941252..20061727hg38UCSC Ensembl
chr21:21313716..21433890hg19UCSC Ensembl
Innerchr21:21313866..21433740hg19UCSC Ensembl
Outerchr21:21313566..21434040hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38120176
hg19120175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16277665
SamplesNA19355
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646538
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