A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390293



Internal ID21047846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112741328..112744556hg38UCSC Ensembl
chr4:113662484..113665712hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383229
hg193229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390293
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