A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225832



Internal ID22368843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13691631..13697682hg38UCSC Ensembl
chr18:13691630..13697681hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg386052
hg196052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14290356
SamplesHG00513
Known GenesFAM210A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225832
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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