A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191070



Internal ID22341832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11916946..11918629hg38UCSC Ensembl
chr1:143181042..143182726hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg381684
hg191685
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302064, nssv14302063, nssv14302062, nssv14302058, nssv14302056, nssv14302057, nssv14302060, nssv14302059, nssv14302061
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)nsv3191070
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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