A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215977



Internal ID20783017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165174712..165181447hg38UCSC Ensembl
chr5:164601718..164608453hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg386736
hg196736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215977
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00166


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