A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701489



Internal ID125155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37367451..37367600hg38UCSC Ensembl
chr15:37659652..37659801hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701489
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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