A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500197



Internal ID22558134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99487435..99489563hg38UCSC Ensembl
chr5:98823139..98825267hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg382129
hg192129
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500197
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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