A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626897



Internal ID15503743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:152600862..152604878hg38UCSC Ensembl
Outerchr2:153457376..153461392hg19UCSC Ensembl
Outerchr2:153165622..153169638hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg384017
hg194017
hg184017
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513645
Supporting Variants
Samples1
Known GenesFMNL2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626897
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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