A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368749



Internal ID22594418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:122684772..124045529hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381360758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368749
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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