A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497520



Internal ID22555454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98132683..98154365hg38UCSC Ensembl
chr3:97851527..97873209hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3821683
hg1921683
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837480
Supporting Variants
Samples
Known GenesOR5H1, OR5H14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497520
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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