A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757674



Internal ID20533534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76063890..76063890hg38UCSC Ensembl
chr9:78678806..78678806hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288855
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757674
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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