A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201331



Internal ID22350658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26016737..26021167hg38UCSC Ensembl
chr1:26343228..26347658hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384431
hg194431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355449, nssv14355444, nssv14355452, nssv14355451, nssv14355448, nssv14355446, nssv14355445, nssv14355447, nssv14355450
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)nsv3201331
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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