A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208293



Internal ID20775333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201442349..201450325hg38UCSC Ensembl
chr2:202307072..202315048hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg387977
hg197977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346208
Supporting Variants
Samples
Known GenesTRAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208293
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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