A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998145



Internal ID19194010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15675161..15777717hg38UCSC Ensembl
Outerchr19:15785971..15888527hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38102557
hg19102557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153107
Supporting Variants
SamplesKWB1
Known GenesCYP4F12, CYP4F24P, OR10H2, OR10H3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998145
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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