A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343003



Internal ID21000556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219677197..219686946hg38UCSC Ensembl
chr2:220541919..220551668hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg389750
hg199750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343003
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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