A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116602



Internal ID20683642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32062630..32067459hg38UCSC Ensembl
chr4:32064252..32069081hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg384830
hg194830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116602
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