A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040981



Internal ID95032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103828545..103828620hg38UCSC Ensembl
chr10:105588303..105588378hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509512
Supporting Variants
Samples
Known GenesSH3PXD2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040981
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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