A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021659



Internal ID22083290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77852359..77876112hg38UCSC Ensembl
Outerchr6:77845174..77883980hg38UCSC Ensembl
Innerchr6:78562076..78585829hg19UCSC Ensembl
Outerchr6:78554891..78593697hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3838807
hg1938807
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156540
Supporting Variants
Samples
Known GenesMEI4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021659
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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