A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145364



Internal ID21401675
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 StatusS
Merged Variantsnsv5631065
Supporting Variants
SamplesHG00096
Known GenesHTR1E
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145364
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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