A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512457



Internal ID15505196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89901070..89902778hg38UCSC Ensembl
Outerchr16:89967478..89969186hg19UCSC Ensembl
Outerchr16:88494979..88496687hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381709
hg191709
hg181709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625053
Samples1
Known GenesTCF25
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512457
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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