A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374577



Internal ID21032130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46442520..46444404hg38UCSC Ensembl
chr3:46484011..46485895hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381885
hg191885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209282
Samples
Known GenesLTF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374577
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