A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529598



Internal ID22398990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93335574..93335628hg38UCSC Ensembl
chr10:95095331..95095385hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14356321, nssv14356320, nssv14356322
SamplesNA19238, HG00732, HG00733
Known GenesMYOF
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529598
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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