A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512112



Internal ID15851537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:103566258..103570828hg38UCSC Ensembl
Outerchr9:106328540..106333110hg19UCSC Ensembl
Outerchr9:105368361..105372931hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg384571
hg194571
hg184571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624670
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)nsv512112
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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