A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096534



Internal ID20663574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157556601..157559500hg38UCSC Ensembl
chr3:157274390..157277289hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365178
Supporting Variants
Samples
Known GenesC3orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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