A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622307



Internal ID7009166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9449013..9454549hg38UCSC Ensembl
Innerchr10:9449013..9454549hg38UCSC Ensembl
Outerchr10:9448994..9454709hg38UCSC Ensembl
chr10:9490976..9496512hg19UCSC Ensembl
Innerchr10:9490976..9496512hg19UCSC Ensembl
Outerchr10:9490957..9496672hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385537
hg195537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13691671
SamplesHG01190
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622307
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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