A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158796



Internal ID20725836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76175349..76179206hg38UCSC Ensembl
chr7:75804667..75808524hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158796
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