A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336364



Internal ID20993917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199548575..199549260hg38UCSC Ensembl
chr2:200413298..200413983hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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