A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644489



Internal ID21592794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52995787..52995787hg38UCSC Ensembl
chr6:52860585..52860585hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158843
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644489
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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