A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007201



Internal ID22068832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71479586..71481754hg38UCSC Ensembl
Outerchr11:71471313..71484605hg38UCSC Ensembl
Innerchr11:71190632..71192800hg19UCSC Ensembl
Outerchr11:71182359..71195651hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3813293
hg1913293
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154747
Supporting Variants
Samples
Known GenesMIR6754, NADSYN1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007201
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