A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624538



Internal ID6664702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110252088..110255060hg38UCSC Ensembl
Innerchr10:110252088..110255060hg38UCSC Ensembl
Outerchr10:110251884..110255236hg38UCSC Ensembl
chr10:112011846..112014818hg19UCSC Ensembl
Innerchr10:112011846..112014818hg19UCSC Ensembl
Outerchr10:112011642..112014994hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382973
hg192973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13933958, essv13933960, essv13933961, essv13933962, essv13933959
SamplesNA19712, HG02722, HG03088, HG01912, NA20339
Known GenesMXI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624538
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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