A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486532



Internal ID22544447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162045480..162055501hg38UCSC Ensembl
chr3:161763268..161773289hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3810022
hg1910022
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835061
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486532
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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