A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362045



Internal ID22587714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232229701..232234614hg38UCSC Ensembl
chr1:232365447..232370360hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg384914
hg194914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362045
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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