A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209697



Internal ID20776737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146036203..146046095hg38UCSC Ensembl
chr3:145753990..145763882hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg389893
hg199893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209697
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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