A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212353



Internal ID20779393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73832201..73841000hg38UCSC Ensembl
chr4:74697918..74706717hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391931
Supporting Variants
Samples
Known GenesCXCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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