A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349439



Internal ID21006992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167293248..167340358hg38UCSC Ensembl
chr2:168149758..168196868hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3847111
hg1947111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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