A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121298



Internal ID20688338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99111307..99116097hg38UCSC Ensembl
chr4:100032458..100037248hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg384791
hg194791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382190
Supporting Variants
Samples
Known GenesLOC100507053
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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