A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211413



Internal ID20778453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150240429..150241367hg38UCSC Ensembl
chr3:149958216..149959154hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211413
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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