A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921963



Internal ID22697187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66208512..66209479hg38UCSC Ensembl
chr8:67120747..67121714hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921963
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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