A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702075



Internal ID125741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75504733..75504926hg38UCSC Ensembl
chr15:75797074..75797267hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523818
Supporting Variants
Samples
Known GenesPTPN9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702075
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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