A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492197



Internal ID22550124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98261103..98266520hg38UCSC Ensembl
chr3:97979947..97985364hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg385418
hg195418
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837255
Supporting Variants
Samples
Known GenesOR5H6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492197
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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