A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701094



Internal ID124760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41171687..41172770hg38UCSC Ensembl
chr15:41463885..41464968hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381084
hg191084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701094
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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