A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512765



Internal ID289312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39466824..39479233hg38UCSC Ensembl
chr15:39759025..39771434hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3812410
hg1912410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512765
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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