A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971178



Internal ID22746113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98437709..98437709hg38UCSC Ensembl
chr15:98980938..98980938hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381262
Samples
Known GenesFAM169B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971178
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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