A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487022



Internal ID22544937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164848979..164869923hg38UCSC Ensembl
chr3:164566767..164587711hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3820945
hg1920945
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487022
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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