A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923495



Internal ID22698722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13615228..13679075hg38UCSC Ensembl
chr8:13472737..13536584hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3863848
hg1963848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923495
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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