A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513103



Internal ID15852525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:194400309..194401253hg38UCSC Ensembl
Outerchr3:194121038..194121982hg19UCSC Ensembl
Outerchr3:195602327..195603271hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38945
hg19945
hg18945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626593
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)nsv513103
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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