A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702428



Internal ID126094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72227763..72227889hg38UCSC Ensembl
chr15:72520104..72520230hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531968
Supporting Variants
Samples
Known GenesPKM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702428
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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