A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225609



Internal ID20792649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94027609..94040006hg38UCSC Ensembl
chr7:93656921..93669318hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3812398
hg1912398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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