A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214179



Internal ID20781219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79179915..79187108hg38UCSC Ensembl
chr5:78475738..78482931hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg387194
hg197194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214179
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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