A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916151



Internal ID22691370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121606546..121610078hg38UCSC Ensembl
chr8:122618786..122622318hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg383533
hg193533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916151
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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