A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623725



Internal ID21815772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44645190..44645422hg38UCSC Ensembl
chr19:45148471..45148693hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38233
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058518
Supporting Variants
Samples
Known GenesPVR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623725
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer