A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232369



Internal ID20799409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130530551..130539488hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00061


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