A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623851



Internal ID6664018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75436041..75441393hg38UCSC Ensembl
Innerchr10:75436068..75441367hg38UCSC Ensembl
Outerchr10:75436015..75441420hg38UCSC Ensembl
chr10:77195799..77201151hg19UCSC Ensembl
Innerchr10:77195826..77201125hg19UCSC Ensembl
Outerchr10:77195773..77201178hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg385353
hg195353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863970
SamplesNA18949
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623851
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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