A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925488



Internal ID22700715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8668527..8668577hg38UCSC Ensembl
chr8:8526037..8526087hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925488
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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