A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216188



Internal ID22362267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27363484..27363609hg38UCSC Ensembl
chr15:27608630..27608755hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380956, nssv14383376, nssv14376760
SamplesHG00512, HG00513, HG00514
Known GenesGABRG3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216188
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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