A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529648



Internal ID22399039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87394789..87395022hg38UCSC Ensembl
chr16:87428395..87428628hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14389565, nssv14379236, nssv14384217
SamplesNA19238, HG00731, HG00514
Known GenesMAP1LC3B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529648
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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