A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701122



Internal ID124788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41343977..41344355hg38UCSC Ensembl
chr15:41636175..41636553hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501871
Supporting Variants
Samples
Known GenesNUSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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