A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397830



Internal ID22455700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17150571..17151004hg38UCSC Ensembl
chr19:17261381..17261814hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940462
Supporting Variants
Samples
Known GenesMYO9B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397830
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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