A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348545



Internal ID21006098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28706839..28723569hg38UCSC Ensembl
chr2:28929705..28946435hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3816731
hg1916731
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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