A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361164



Internal ID21018717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37934..135299hg38UCSC Ensembl
chr4:37935..129044hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3897366
hg1991110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213551
Samples
Known GenesZNF595, ZNF718
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361164
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