A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499398



Internal ID276372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31459808..31467078hg38UCSC Ensembl
chr15:31752011..31759281hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg387271
hg197271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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