A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415201



Internal ID22473071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154520372..154525752hg38UCSC Ensembl
chr5:153899932..153905312hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg385381
hg195381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415201
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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