A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513667



Internal ID15853088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:106719101..106723596hg38UCSC Ensembl
Outerchr6:107166976..107171471hg19UCSC Ensembl
Outerchr6:107273669..107278164hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384496
hg194496
hg184496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626919
Samples1
Known GenesLOC100422737
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513667
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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