A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353309



Internal ID21010862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74116012..74129020hg38UCSC Ensembl
chr2:74343139..74356147hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg3813009
hg1913009
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353309
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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