A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624665



Internal ID15501515
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 StatusS
Merged Variantsnsv512108
Supporting Variants
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)nssv624665
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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