A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190631



Internal ID22341467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17718417..17720049hg38UCSC Ensembl
chr21:19090735..19092367hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381633
hg191633
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301580, nssv14301576, nssv14301577, nssv14301573, nssv14301572, nssv14301574, nssv14301578, nssv14301575, nssv14301579
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)nsv3190631
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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