A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476706



Internal ID22534604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44667511..44670143hg38UCSC Ensembl
chr19:45170779..45173415hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg382633
hg192637
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476706
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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