A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513789



Internal ID290303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35081634..35082500hg38UCSC Ensembl
chr15:35373835..35374701hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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