A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14860944



Internal ID4193243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93157107..93158434hg38UCSC Ensembl
Innerchr13:93157117..93158424hg38UCSC Ensembl
Outerchr13:93157097..93158444hg38UCSC Ensembl
chr13:93809360..93810687hg19UCSC Ensembl
Innerchr13:93809370..93810677hg19UCSC Ensembl
Outerchr13:93809350..93810697hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633189
Supporting Variants
SamplesHG03781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14860944
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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