A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631688



Internal ID7018496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31006697..31009509hg38UCSC Ensembl
Innerchr13:31006731..31009475hg38UCSC Ensembl
Outerchr13:31006663..31009543hg38UCSC Ensembl
chr13:31580834..31583646hg19UCSC Ensembl
Innerchr13:31580868..31583612hg19UCSC Ensembl
Outerchr13:31580800..31583680hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382813
hg192813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14682697
SamplesHG00407
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631688
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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