A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626574



Internal ID15850107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:148562638..148567845hg38UCSC Ensembl
Outerchr3:148280425..148285632hg19UCSC Ensembl
Outerchr3:149763115..149768322hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385208
hg195208
hg185208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513087
Supporting Variants
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)nssv626574
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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