A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342760



Internal ID21000313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219701154..219713360hg38UCSC Ensembl
chr2:220565876..220578082hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3812207
hg1912207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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