A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922897



Internal ID22698122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94712939..94715995hg38UCSC Ensembl
chr8:95725167..95728223hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383057
hg193057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922897
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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