A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225345



Internal ID22368503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88331841..88339671hg38UCSC Ensembl
chr16:88365447..88373277hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg387831
hg197831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383740, nssv14379555, nssv14390012
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225345
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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