A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863970



Internal ID3865786
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623851
Supporting Variants
SamplesNA18949
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863970
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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