A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705533



Internal ID129199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88635723..88635791hg38UCSC Ensembl
chr15:89178954..89179022hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705533
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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