A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916880



Internal ID22692099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127898081..127898224hg38UCSC Ensembl
chr8:128910327..128910470hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435213
Samples
Known GenesPVT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916880
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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