A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210233



Internal ID22358187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8026925..8027022hg38UCSC Ensembl
chr1:8086985..8087082hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313799, nssv14313798, nssv14313800
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210233
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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