A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379943



Internal ID21037496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86845822..86949507hg38UCSC Ensembl
chr4:87766975..87870659hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38103686
hg19103685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214753
Samples
Known GenesAFF1, C4orf36, LOC100506746, SLC10A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379943
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