A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608065



Internal ID20981136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23475684..23493498hg38UCSC Ensembl
chr7:23515303..23533117hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817815
hg1917815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232269
Samples
Known GenesRPS2P32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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