A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513664



Internal ID15853085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:12429214..12432194hg38UCSC Ensembl
Outerchr6:12429446..12432426hg19UCSC Ensembl
Outerchr6:12537432..12540412hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg382981
hg192981
hg182981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626916
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513664
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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