A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211436



Internal ID22358999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62550152..62748179hg38UCSC Ensembl
chr9:46861453..47059480hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38198028
hg19198028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346101, nssv14346098, nssv14346100, nssv14346097, nssv14346096, nssv14346099, nssv14346102, nssv14346104, nssv14346103
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)nsv3211436
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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