A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368789



Internal ID21026342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99563784..99568700hg38UCSC Ensembl
chr3:99282628..99287544hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg384917
hg194917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211309
Samples
Known GenesMIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368789
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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