A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528893



Internal ID304933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97410093..97410392hg38UCSC Ensembl
chr15:97953323..97953622hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528893
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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