A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490043



Internal ID22547964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184671039..184672066hg38UCSC Ensembl
chr3:184388827..184389854hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381028
hg191028
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490043
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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