A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513078



Internal ID15852500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:140548665..140552044hg38UCSC Ensembl
Outerchr3:140267507..140270886hg19UCSC Ensembl
Outerchr3:141750197..141753576hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383380
hg193380
hg183380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626564
Samples1
Known GenesCLSTN2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513078
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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