A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490539



Internal ID22548463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24128161..24129186hg38UCSC Ensembl
chr3:24169652..24170677hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835554
Supporting Variants
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490539
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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