A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221179



Internal ID22365652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130197851..130203300hg38UCSC Ensembl
chr10:131996115..132001564hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385450
hg195450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1111n152
Supporting Variantsnssv14356733, nssv14356736, nssv14356729, nssv14356734, nssv14356730, nssv14356728, nssv14356731, nssv14356735, nssv14356732
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)nsv3221179
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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