A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391874



Internal ID21049427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87052864..87057333hg38UCSC Ensembl
chr4:87974016..87978485hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg384470
hg194470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121761
Samples
Known GenesAFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer