A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358908



Internal ID21016461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2377846..2398633hg38UCSC Ensembl
chr4:2379573..2400360hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3820788
hg1920788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5132n223
Supporting Variantsnssv18211774
Samples
Known GenesZFYVE28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358908
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