A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513176



Internal ID15505912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:166081570..166084416hg38UCSC Ensembl
Outerchr4:167002722..167005568hg19UCSC Ensembl
Outerchr4:167222172..167225018hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382847
hg192847
hg182847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626673
Samples1
Known GenesTLL1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513176
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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