A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225400



Internal ID22368539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61894851..61895950hg38UCSC Ensembl
chr18:59562084..59563183hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3884n152
Supporting Variantsnssv14285524, nssv14285526, nssv14285531, nssv14285527, nssv14285530, nssv14285525, nssv14285529, nssv14285528, nssv14285523
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225400
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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