A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13757267



Internal ID3480768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38153794..38162362hg38UCSC Ensembl
Innerchr10:38154294..38161862hg38UCSC Ensembl
Outerchr10:38152794..38163362hg38UCSC Ensembl
chr10:38442722..38451290hg19UCSC Ensembl
Innerchr10:38443222..38450790hg19UCSC Ensembl
Outerchr10:38441722..38452290hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg388569
hg198569
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622977
Supporting Variants
SamplesHG03096
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13757267
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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