A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347379



Internal ID21004932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219956066..219966415hg38UCSC Ensembl
chr2:220820787..220831136hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3810350
hg1910350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347379
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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