A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921463



Internal ID22696687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114082728..114087900hg38UCSC Ensembl
chr8:115094957..115100129hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg385173
hg195173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921463
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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