A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911803



Internal ID22687018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107158322..107166744hg38UCSC Ensembl
chr8:108170550..108178972hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg388423
hg198423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911803
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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