A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121479



Internal ID20688519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97149940..97150601hg38UCSC Ensembl
chr4:98071091..98071752hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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