A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908007



Internal ID22683217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86270848..86276727hg38UCSC Ensembl
chr8:87283077..87288956hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385880
hg195880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908007
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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