A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209641



Internal ID20776681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141396401..141402200hg38UCSC Ensembl
chr3:141115243..141121042hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356816
Supporting Variants
Samples
Known GenesZBTB38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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