A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491467



Internal ID22549392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39876734..39885795hg38UCSC Ensembl
chr3:39918225..39927286hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389062
hg199062
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836194
Supporting Variants
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491467
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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