A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624911



Internal ID15848447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:73500534..73501657hg38UCSC Ensembl
Outerchr13:74074671..74075794hg19UCSC Ensembl
Outerchr13:72972672..72973795hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381124
hg191124
hg181124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512329
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)nssv624911
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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