A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184269



Internal ID21323065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87332617..87332617hg38UCSC Ensembl
chr16:87366223..87366223hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942549
Supporting Variants
SamplesHG002
Known GenesFBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184269
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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