A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225328



Internal ID20792368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85667392..85791737hg38UCSC Ensembl
chr7:85296708..85421053hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38124346
hg19124346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225328
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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