A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512108



Internal ID15504847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91795707..91799271hg38UCSC Ensembl
Outerchr9:94557989..94561553hg19UCSC Ensembl
Outerchr9:93597810..93601374hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383565
hg193565
hg183565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624665
Samples1
Known GenesROR2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512108
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer