A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151482



Internal ID20718522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15689201..15691500hg38UCSC Ensembl
chr7:15728826..15731125hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0014


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