A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633531



Internal ID7020340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109707186..109731351hg38UCSC Ensembl
chr13:110359533..110383698hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3824166
hg1924166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv370e214
Supporting Variantsessv14895670, essv14895669, essv14895668
SamplesHG04210, HG00737, HG00553
Known GenesLINC00676
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633531
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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