A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13973287



Internal ID3975103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129481084..129487991hg38UCSC Ensembl
Innerchr10:129481084..129487991hg38UCSC Ensembl
Outerchr10:129480911..129488126hg38UCSC Ensembl
chr10:131279348..131286255hg19UCSC Ensembl
Innerchr10:131279348..131286255hg19UCSC Ensembl
Outerchr10:131279175..131286390hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386908
hg196908
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624921
Supporting Variants
SamplesHG01051
Known GenesMGMT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13973287
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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