A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842158



Internal ID22617093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163793012..163798503hg38UCSC Ensembl
chr5:163220018..163225509hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385492
hg195492
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842158
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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