A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764321



Internal ID6031329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43490555..43492494hg38UCSC Ensembl
Innerchr10:43490581..43492468hg38UCSC Ensembl
Outerchr10:43490529..43492520hg38UCSC Ensembl
chr10:43986003..43987942hg19UCSC Ensembl
Innerchr10:43986029..43987916hg19UCSC Ensembl
Outerchr10:43985977..43987968hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381940
hg191940
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623046
Supporting Variants
SamplesNA19437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764321
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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