A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631437



Internal ID7018246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20881516..20884006hg38UCSC Ensembl
Innerchr13:20881566..20883956hg38UCSC Ensembl
Outerchr13:20881434..20884088hg38UCSC Ensembl
chr13:21455655..21458145hg19UCSC Ensembl
Innerchr13:21455705..21458095hg19UCSC Ensembl
Outerchr13:21455573..21458227hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382491
hg192491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14658395, essv14658396
SamplesNA19917, NA20764
Known GenesXPO4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631437
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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