A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208917



Internal ID20775957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1039074..1102977hg38UCSC Ensembl
chr3:1080758..1144661hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3863904
hg1963904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364606
Supporting Variants
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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