A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442019



Internal ID22499889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20574822..20574907hg38UCSC Ensembl
chr8:20432333..20432418hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925550
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442019
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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