A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359588



Internal ID21017141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99276552..99578591hg38UCSC Ensembl
chr3:98995396..99297435hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38302040
hg19302040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211305
Samples
Known GenesMIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359588
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer