A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513042



Internal ID15852464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:36015258..36016801hg38UCSC Ensembl
Outerchr3:36056750..36058293hg19UCSC Ensembl
Outerchr3:36031754..36033297hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381544
hg191544
hg181544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626525
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)nsv513042
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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