A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041625



Internal ID20608665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59674484..59936666hg38UCSC Ensembl
chr18:57341716..57603898hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38262183
hg19262183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516670
Supporting Variants
Samples
Known GenesCCBE1, PMAIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041625
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