A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107699



Internal ID20674739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10863359..10872233hg38UCSC Ensembl
chr4:10864983..10873857hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg388875
hg198875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357139
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107699
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