A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513088



Internal ID15852510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:152593823..152595572hg38UCSC Ensembl
Outerchr3:152311612..152313361hg19UCSC Ensembl
Outerchr3:153794302..153796051hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381750
hg191750
hg181750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626575
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)nsv513088
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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