A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632569



Internal ID7019379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67786974..67800348hg38UCSC Ensembl
Innerchr13:67787474..67799848hg38UCSC Ensembl
Outerchr13:67785974..67801348hg38UCSC Ensembl
chr13:68361106..68374480hg19UCSC Ensembl
Innerchr13:68361606..68373980hg19UCSC Ensembl
Outerchr13:68360106..68375480hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3813375
hg1913375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv344e214
Supporting Variantsessv14782230
SamplesHG00704
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632569
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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