A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203294



Internal ID22352334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190561296..190563051hg38UCSC Ensembl
chr2:191426022..191427777hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg381756
hg191756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14295310, nssv14295308, nssv14295313, nssv14295309, nssv14295306, nssv14295307, nssv14295305, nssv14295311, nssv14295312
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)nsv3203294
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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