A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232269



Internal ID20799309
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 StatusS
Merged Variantsnsv6608065
Supporting Variants
Samples
Known GenesRPS2P32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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