A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623857



Internal ID6664024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75824039..75829697hg38UCSC Ensembl
Innerchr10:75824039..75829697hg38UCSC Ensembl
Outerchr10:75823777..75829940hg38UCSC Ensembl
chr10:77583797..77589455hg19UCSC Ensembl
Innerchr10:77583797..77589455hg19UCSC Ensembl
Outerchr10:77583535..77589698hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg385659
hg195659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13864454
SamplesHG02053
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623857
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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