A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339653



Internal ID20997206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202334049..202362566hg38UCSC Ensembl
chr2:203198772..203227289hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3828518
hg1928518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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