A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124011



Internal ID20691052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105826069..105915444hg38UCSC Ensembl
chr5:105161770..105251145hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3889376
hg1989376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124011
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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