A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626907



Internal ID15850439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:40232453..40234874hg38UCSC Ensembl
Outerchr4:40234073..40236494hg19UCSC Ensembl
Outerchr4:39910468..39912889hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382422
hg192422
hg182422
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513655
Supporting Variants
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)nssv626907
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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