A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626889



Internal ID15850421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:91663019..91667052hg38UCSC Ensembl
Outerchr1:92128576..92132609hg19UCSC Ensembl
Outerchr1:91901164..91905197hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg384034
hg194034
hg184034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513637
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)nssv626889
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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