A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14895846



Internal ID1352275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110088763..110111130hg38UCSC Ensembl
Innerchr13:110088913..110110980hg38UCSC Ensembl
Outerchr13:110088613..110111280hg38UCSC Ensembl
chr13:110741110..110763477hg19UCSC Ensembl
Innerchr13:110741260..110763327hg19UCSC Ensembl
Outerchr13:110740960..110763627hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3822368
hg1922368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633541
Supporting Variants
SamplesHG01190
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14895846
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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