A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426375



Internal ID205311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23765111..23765310hg38UCSC Ensembl
chr1:24091601..24091800hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901107
Samples
Known GenesLOC100506963
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426375
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