A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525379



Internal ID301541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83769697..83771132hg38UCSC Ensembl
chr15:84438449..84439884hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702602
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525379
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer