A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367055



Internal ID22592724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:122859779..124480561hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381620783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367055
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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