A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364402



Internal ID21021955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4783374..5226266hg38UCSC Ensembl
chr4:4785101..5227993hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38442893
hg19442893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211879
Samples
Known GenesCYTL1, MSX1, STK32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364402
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