A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372323



Internal ID21029876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2340316..2341106hg38UCSC Ensembl
chr4:2342043..2342833hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114683
Samples
Known GenesZFYVE28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372323
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