A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224963



Internal ID20792003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25255173..25264438hg38UCSC Ensembl
chr7:25294792..25304057hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg389266
hg199266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612640
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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