A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125230



Internal ID20692270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128058115..128058700hg38UCSC Ensembl
chr5:127393807..127394392hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402726
Supporting Variants
Samples
Known GenesFLJ33630
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125230
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00105


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