A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911883



Internal ID22687098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75208820..75210214hg38UCSC Ensembl
chr8:76121055..76122449hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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