A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107786



Internal ID20674826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109963966..109964515hg38UCSC Ensembl
chr4:110885122..110885671hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386313
Supporting Variants
Samples
Known GenesEGF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer