A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039825



Internal ID94275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98387590..98387689hg38UCSC Ensembl
chr10:100147347..100147446hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476287
Supporting Variants
Samples
Known GenesPYROXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039825
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001717


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