A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641146



Internal ID21589451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136074452..136074452hg38UCSC Ensembl
chr9:138966298..138966298hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160878
SamplesHG00731
Known GenesNACC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641146
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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