A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654187



Internal ID21602492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89536469..89536469hg38UCSC Ensembl
chr16:89602877..89602877hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097141
SamplesHG00731
Known GenesSPG7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654187
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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