A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437768



Internal ID22495638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17346274..17346342hg38UCSC Ensembl
chr9:17346272..17346340hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920514
Supporting Variants
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437768
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