A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13883021



Internal ID3884837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86118407..86120236hg38UCSC Ensembl
Innerchr10:86118457..86120186hg38UCSC Ensembl
Outerchr10:86118353..86120290hg38UCSC Ensembl
chr10:87878164..87879993hg19UCSC Ensembl
Innerchr10:87878214..87879943hg19UCSC Ensembl
Outerchr10:87878110..87880047hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381830
hg191830
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624083
Supporting Variants
SamplesHG00610
Known GenesGRID1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13883021
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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