A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129306



Internal ID20696346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:23066318..23075245hg38UCSC Ensembl
chr5:23066427..23075354hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg388928
hg198928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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