A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13882076



Internal ID1036728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84586296..84621371hg38UCSC Ensembl
Innerchr10:84586359..84621308hg38UCSC Ensembl
Outerchr10:84586233..84621434hg38UCSC Ensembl
chr10:86346052..86381127hg19UCSC Ensembl
Innerchr10:86346115..86381064hg19UCSC Ensembl
Outerchr10:86345989..86381190hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3835076
hg1935076
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624037
Supporting Variants
SamplesHG00656
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13882076
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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