A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624921



Internal ID6665083
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13973287
SamplesHG01051
Known GenesMGMT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624921
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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