A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214957



Internal ID20781997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86314901..86419000hg38UCSC Ensembl
chr5:85610719..85714817hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38104100
hg19104099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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