A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626967



Internal ID15850499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:25999631..26002353hg38UCSC Ensembl
Outerchr21:27371946..27374668hg19UCSC Ensembl
Outerchr21:26293817..26296539hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg382723
hg192723
hg182723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513715
Supporting Variants
Samples1
Known GenesAPP
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626967
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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