A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490966



Internal ID22548891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24918374..24977836hg38UCSC Ensembl
chr3:24959865..25019327hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3859463
hg1959463
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490966
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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