A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119428



Internal ID20686468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6690768..6697288hg38UCSC Ensembl
chr4:6692495..6699015hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386521
hg196521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361067
Supporting Variants
Samples
Known GenesS100P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119428
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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