A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401218



Internal ID22459088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141848944..141855877hg38UCSC Ensembl
chr3:141567786..141574719hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386934
hg196934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401218
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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