A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624659



Internal ID15501509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123086..69128466hg38UCSC Ensembl
Outerchr9:71738002..71743382hg19UCSC Ensembl
Outerchr9:70927822..70933202hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385381
hg195381
hg185381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512102
Supporting Variants
Samples1
Known GenesTJP2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624659
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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