A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465159



Internal ID22523048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169470254..169472023hg38UCSC Ensembl
chr1:169439492..169441261hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381770
hg191770
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828724
Supporting Variants
Samples
Known GenesSLC19A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465159
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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