A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420513



Internal ID22478383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169471521..169471588hg38UCSC Ensembl
chr5:168898525..168898592hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897788
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420513
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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