A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512841



Internal ID15852263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:185826762..185827288hg38UCSC Ensembl
Outerchr4:186747916..186748442hg19UCSC Ensembl
Outerchr4:186984910..186985436hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38980
hg19980
hg18980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625479
Samples1
Known GenesSORBS2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512841
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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