A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924864



Internal ID22700091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93048993..93061931hg38UCSC Ensembl
chr8:94061221..94074159hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3812939
hg1912939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924864
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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