A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14898035



Internal ID6855673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110757713..110775989hg38UCSC Ensembl
Innerchr13:110758213..110775489hg38UCSC Ensembl
Outerchr13:110756713..110776989hg38UCSC Ensembl
chr13:111410060..111428336hg19UCSC Ensembl
Innerchr13:111410560..111427836hg19UCSC Ensembl
Outerchr13:111409060..111429336hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3818277
hg1918277
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633549
Supporting Variants
SamplesNA21089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14898035
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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