A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375986



Internal ID21033539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120986474..120997797hg38UCSC Ensembl
chr4:121907629..121918952hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3811324
hg1911324
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375986
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