A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579496



Internal ID21771539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98387588..98387689hg38UCSC Ensembl
chr10:100147345..100147446hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013034
Supporting Variants
Samples
Known GenesPYROXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579496
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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