A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631827



Internal ID21580132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129626106..129626106hg38UCSC Ensembl
chr6:129947251..129947251hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141793
SamplesHG00096
Known GenesARHGAP18
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631827
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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