A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512131



Internal ID15851556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137840660..137842832hg38UCSC Ensembl
Outerchr9:140735112..140737284hg19UCSC Ensembl
Outerchr9:139854933..139857105hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382173
hg192173
hg182173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624691
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)nsv512131
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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