A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505537



Internal ID282308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41322790..41325991hg38UCSC Ensembl
chr15:41614988..41618189hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701117
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505537
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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