A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499088



Internal ID276068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34155215..34155275hg38UCSC Ensembl
chr15:34447416..34447476hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700474
Samples
Known GenesKATNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499088
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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