A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361780



Internal ID21019333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139980559..140040307hg38UCSC Ensembl
chr3:139699401..139759149hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3859749
hg1959749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209627
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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