A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624239



Internal ID6664406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93426923..93428244hg38UCSC Ensembl
Innerchr10:93426941..93428227hg38UCSC Ensembl
Outerchr10:93426906..93428262hg38UCSC Ensembl
chr10:95186680..95188001hg19UCSC Ensembl
Innerchr10:95186698..95187984hg19UCSC Ensembl
Outerchr10:95186663..95188019hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381322
hg191322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13899670, essv13899669, essv13899666, essv13899668, essv13899667
SamplesNA19904, HG01075, NA12873, HG00105, NA12717
Known GenesMYOF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624239
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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