A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626903



Internal ID15850435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:128627926..128656634hg38UCSC Ensembl
Outerchr3:128346769..128375477hg19UCSC Ensembl
Outerchr3:129829459..129858167hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3828709
hg1928709
hg1828709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513651
Supporting Variants
Samples1
Known GenesRPN1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626903
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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