A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700152



Internal ID123818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40962144..40962362hg38UCSC Ensembl
chr15:41254342..41254560hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer