A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099786



Internal ID22009019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73112353..73112353hg38UCSC Ensembl
chr10:74872111..74872111hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584838
Samples
Known GenesNUDT13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099786
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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