A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376081



Internal ID21033634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51866801..51869200hg38UCSC Ensembl
chr4:52732967..52735366hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211891
Samples
Known GenesDCUN1D4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376081
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