A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631065



Internal ID21579370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86968908..86968908hg38UCSC Ensembl
chr6:87678626..87678626hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145364
SamplesHG00096
Known GenesHTR1E
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631065
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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