A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473275



Internal ID22531168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15945683..15973501hg38UCSC Ensembl
chr19:16056493..16084311hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3827819
hg1927819
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876502
Supporting Variants
Samples
Known GenesOR10H4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473275
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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