A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513656



Internal ID15853077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:40233453..40236494hg38UCSC Ensembl
Outerchr4:40235073..40238114hg19UCSC Ensembl
Outerchr4:39911468..39914509hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg383042
hg193042
hg183042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626908
Samples1
Known GenesRHOH
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513656
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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