A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485111



Internal ID22543022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135906061..135963661hg38UCSC Ensembl
chr3:135624903..135682503hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3857601
hg1957601
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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