A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906880



Internal ID22682084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118322558..118325921hg38UCSC Ensembl
chr4:119243713..119247076hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383364
hg193364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419512
Samples
Known GenesPRSS12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906880
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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