A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084986



Internal ID21994219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97668125..97668125hg38UCSC Ensembl
chr10:99427882..99427882hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593416
Samples
Known GenesPI4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084986
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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