A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908726



Internal ID22683936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30564868..30564920hg38UCSC Ensembl
chr8:30422385..30422437hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448263
Samples
Known GenesRBPMS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908726
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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