A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129486



Internal ID20696526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167442477..167443202hg38UCSC Ensembl
chr5:166869482..166870207hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403781
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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