A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428322



Internal ID22486192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33368077..33369149hg38UCSC Ensembl
chr5:33368183..33369255hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381073
hg191073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428322
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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