A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491535



Internal ID22549460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4272428..4316287hg38UCSC Ensembl
chr3:4314112..4357971hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3843860
hg1943860
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836549
Supporting Variants
Samples
Known GenesSETMAR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491535
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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