A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705576



Internal ID129242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96974324..96974386hg38UCSC Ensembl
chr15:97517554..97517616hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520476
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705576
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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