A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363037



Internal ID22588706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:122836107..123199206hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38363100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363037
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