A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632840



Internal ID7019651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80463025..80471822hg38UCSC Ensembl
Innerchr13:80463034..80471814hg38UCSC Ensembl
Outerchr13:80463017..80471831hg38UCSC Ensembl
chr13:81037160..81045957hg19UCSC Ensembl
Innerchr13:81037169..81045949hg19UCSC Ensembl
Outerchr13:81037152..81045966hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg388798
hg198798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14814728, essv14814727, essv14814726, essv14814729
SamplesNA19700, HG02281, HG00632, NA19835
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632840
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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