A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703776



Internal ID127442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99510872..99517506hg38UCSC Ensembl
chr15:100051077..100057711hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg386635
hg196635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703776
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002967


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