A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434384



Internal ID22492254
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 StatusS
Merged Variantsnsv5914871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434384
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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