A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214282



Internal ID20781322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85597201..85639200hg38UCSC Ensembl
chr5:84893019..84935018hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3842000
hg1942000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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