A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211027



Internal ID22358723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155733437..155733494hg38UCSC Ensembl
chr7:155526131..155526188hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338766, nssv14338767, nssv14338763, nssv14338765, nssv14338764
SamplesHG00512, NA19239, HG00732, HG00513, HG00514
Known GenesRBM33
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211027
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer