A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381933



Internal ID21039486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75568401..75588000hg38UCSC Ensembl
chr4:76493611..76513210hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3819600
hg1919600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120212
Samples
Known GenesCDKL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381933
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