A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353164



Internal ID21010717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90249201..90303700hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3854500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4037n223
Supporting Variantsnssv18210641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353164
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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