A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914891



Internal ID22690108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39893444..39893854hg38UCSC Ensembl
chr8:39750963..39751373hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914891
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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