A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908402



Internal ID22683612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139872728..139872927hg38UCSC Ensembl
chr8:140884972..140885171hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447489
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908402
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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