A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626551



Internal ID15850084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:111524173..111530212hg38UCSC Ensembl
Outerchr3:111243020..111249059hg19UCSC Ensembl
Outerchr3:112725710..112731749hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg386040
hg196040
hg186040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513066
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)nssv626551
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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