A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635278



Internal ID21583583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73485339..73485339hg38UCSC Ensembl
chr6:74195062..74195062hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158044
SamplesHG00512
Known GenesMTO1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635278
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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