A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343446



Internal ID21000999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202332956..202342393hg38UCSC Ensembl
chr2:203197679..203207116hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg389438
hg199438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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