A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123618



Internal ID20690658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:125392742..125415628hg38UCSC Ensembl
chr5:124728435..124751321hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3822887
hg1922887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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