A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226295



Internal ID20793335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:305093..359419hg38UCSC Ensembl
chr7:345059..399385hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3854327
hg1954327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608904
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00112


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