A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429444



Internal ID208292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25865044..25865265hg38UCSC Ensembl
chr1:26191535..26191756hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902421
Samples
Known GenesPAQR7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429444
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