A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448769



Internal ID22506639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5516627..5516780hg38UCSC Ensembl
chr9:5516627..5516780hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910547
Supporting Variants
Samples
Known GenesPDCD1LG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448769
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