A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596308



Internal ID21788351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94808775..94816580hg38UCSC Ensembl
chr10:96568532..96576337hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg387806
hg197806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011280
Supporting Variants
Samples
Known GenesCYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596308
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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