A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222499



Internal ID20789539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25052587..25090999hg38UCSC Ensembl
chr7:25092206..25130618hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3838413
hg1938413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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