A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626895



Internal ID15850427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:138246286..138250835hg38UCSC Ensembl
Outerchr2:139003856..139008405hg19UCSC Ensembl
Outerchr2:138720326..138724875hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg384550
hg194550
hg184550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513643
Supporting Variants
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)nssv626895
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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