A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417763



Internal ID22475633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154596156..154596940hg38UCSC Ensembl
chr5:153975716..153976500hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417763
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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