A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497480



Internal ID20870687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80694001..80698100hg38UCSC Ensembl
chr15:80986342..80990441hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193897
Samples
Known GenesABHD17C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497480
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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