A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512899



Internal ID15852321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165677234..165678219hg38UCSC Ensembl
Outerchr6:166090722..166091707hg19UCSC Ensembl
Outerchr6:166010712..166011697hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38951
hg19951
hg18951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625545
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512899
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