A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626979



Internal ID21575284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99478511..99478511hg38UCSC Ensembl
chr6:99926387..99926387hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381998
hg191998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152065
SamplesHG01505
Known GenesUSP45
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626979
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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