A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376385



Internal ID21033938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126199101..126207400hg38UCSC Ensembl
chr4:127120256..127128555hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376385
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