A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13941249



Internal ID2241698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113667320..113674902hg38UCSC Ensembl
Innerchr10:113667368..113674855hg38UCSC Ensembl
Outerchr10:113667273..113674950hg38UCSC Ensembl
chr10:115427079..115434661hg19UCSC Ensembl
Innerchr10:115427127..115434614hg19UCSC Ensembl
Outerchr10:115427032..115434709hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg387583
hg197583
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624606
Supporting Variants
SamplesHG02012
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13941249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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