A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511853



Internal ID15851278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:18400954..18403086hg38UCSC Ensembl
Outerchr6:18401185..18403317hg19UCSC Ensembl
Outerchr6:18509164..18511296hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382133
hg192133
hg182133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624383
Samples1
Known GenesRNF144B
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511853
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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