A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966693



Internal ID22741628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76716027..76716027hg38UCSC Ensembl
chr9:79330943..79330943hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443760
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966693
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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