A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919506



Internal ID22694728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140272036..140272298hg38UCSC Ensembl
chr8:141282135..141282397hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448033
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919506
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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