A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514964



Internal ID291452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31636923..31637015hg38UCSC Ensembl
chr19:32127829..32127921hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv245n206
Supporting Variantsnssv17722769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514964
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