A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129079



Internal ID20696119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24446748..24455809hg38UCSC Ensembl
chr5:24446857..24455918hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg389062
hg199062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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