A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624422



Internal ID7011277
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13915153
SamplesHG00102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624422
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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