A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914871



Internal ID22690088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94366789..94369353hg38UCSC Ensembl
chr8:95379017..95381581hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382565
hg192565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914871
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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