A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409612



Internal ID22467482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139780460..139780516hg38UCSC Ensembl
chr3:139499302..139499358hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409612
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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