A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951461



Internal ID22674944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125155904..125155904hg38UCSC Ensembl
chr9:127918183..127918183hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449215
Samples
Known GenesPPP6C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951461
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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