A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625125



Internal ID15501975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26247132..26249196hg38UCSC Ensembl
Outerchr18:23827096..23829160hg19UCSC Ensembl
Outerchr18:22081094..22083158hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382065
hg192065
hg182065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512522
Supporting Variants
Samples1
Known GenesTAF4B
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625125
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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