A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13915153



Internal ID362679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103928360..103933581hg38UCSC Ensembl
Innerchr10:103928378..103933563hg38UCSC Ensembl
Outerchr10:103928342..103933599hg38UCSC Ensembl
chr10:105688118..105693339hg19UCSC Ensembl
Innerchr10:105688136..105693321hg19UCSC Ensembl
Outerchr10:105688100..105693357hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg385222
hg195222
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624422
Supporting Variants
SamplesHG00102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13915153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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