A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018578



Internal ID21927921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98407725..98407784hg38UCSC Ensembl
chr10:100167482..100167541hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590011
Samples
Known GenesPYROXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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