A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197650



Internal ID22347502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61213566..61215185hg38UCSC Ensembl
chr9:43605556..43607176hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381620
hg191621
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346078, nssv14346071, nssv14346079, nssv14346075, nssv14346072, nssv14346074, nssv14346073, nssv14346076, nssv14346077
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)nsv3197650
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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