A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757292



Internal ID20533152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43541140..43541140hg38UCSC Ensembl
chr5:43541242..43541242hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261593
Samples
Known GenesPAIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757292
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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