A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489858



Internal ID22547779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194515277..194522646hg38UCSC Ensembl
chr3:194236006..194243375hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg387370
hg197370
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489858
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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