A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208995



Internal ID22357140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11919903..11921448hg38UCSC Ensembl
chr1:143178214..143179768hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg381546
hg191555
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302074, nssv14302073, nssv14302068, nssv14302072, nssv14302069, nssv14302071, nssv14302070, nssv14302066, nssv14302067
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)nsv3208995
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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