A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512111



Internal ID15851536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:101681441..101682577hg38UCSC Ensembl
Outerchr9:104443723..104444859hg19UCSC Ensembl
Outerchr9:103483544..103484680hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381137
hg191137
hg181137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624669
Samples1
Known GenesGRIN3A
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512111
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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