A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356320



Internal ID22210128
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529598
Supporting Variants
SamplesHG00732
Known GenesMYOF
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356320
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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