A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917678



Internal ID22692898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93500051..93500563hg38UCSC Ensembl
chr8:94512279..94512791hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442953
Samples
Known GenesLINC00535
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917678
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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