A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235274



Internal ID20802314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21565845..21597650hg38UCSC Ensembl
chr7:21605463..21637268hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3831806
hg1931806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607870
Supporting Variants
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235274
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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