A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525489



Internal ID22394867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86345409..86352111hg38UCSC Ensembl
chr16:86379015..86385717hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386703
hg196703
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392288, nssv14387946
SamplesHG00731, HG00733
Known GenesLINC00917
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525489
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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