A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425135



Internal ID204105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63922476..63924021hg38UCSC Ensembl
chr1:64388147..64389692hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16904212
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425135
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