A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425256



Internal ID22483126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159489106..159491105hg38UCSC Ensembl
chr5:158916114..158918113hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425256
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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