A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632564



Internal ID7019374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67706785..67710614hg38UCSC Ensembl
Innerchr13:67706811..67710589hg38UCSC Ensembl
Outerchr13:67706760..67710640hg38UCSC Ensembl
chr13:68280917..68284746hg19UCSC Ensembl
Innerchr13:68280943..68284721hg19UCSC Ensembl
Outerchr13:68280892..68284772hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg383830
hg193830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14782206, essv14782205
SamplesHG03772, HG03861
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632564
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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