A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129533



Internal ID20696573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16851895..16854817hg38UCSC Ensembl
chr5:16852004..16854926hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382923
hg192923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381326
Supporting Variants
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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