A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356125



Internal ID22581794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168318753..168320913hg38UCSC Ensembl
chr1:168287991..168290151hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382161
hg192161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356125
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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