A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117093



Internal ID20684133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40224043..40224578hg38UCSC Ensembl
chr4:40225663..40226198hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382280
Supporting Variants
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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