A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512097



Internal ID15851522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:32708852..32729848hg38UCSC Ensembl
Outerchr9:32708850..32729846hg19UCSC Ensembl
Outerchr9:32698850..32719846hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3820997
hg1920997
hg1820997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624653
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)nsv512097
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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