A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339982



Internal ID20997535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:192354934..192461515hg38UCSC Ensembl
chr2:193219660..193326241hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38106582
hg19106582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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