A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425771



Internal ID204726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32941220..32941992hg38UCSC Ensembl
chr1:33406821..33407593hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903671
Samples
Known GenesRNF19B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425771
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