A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093174



Internal ID20660214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128632694..128646733hg38UCSC Ensembl
chr3:128351537..128365576hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3814040
hg1914040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370616
Supporting Variants
Samples
Known GenesRPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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