A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380184



Internal ID21037737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75730901..75739600hg38UCSC Ensembl
chr4:76656085..76664784hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212376
Samples
Known GenesUSO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380184
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