A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987804



Internal ID18875681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15675165..15904579hg38UCSC Ensembl
Outerchr19:15785975..16015389hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38229415
hg19229415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133007
Supporting Variants
SamplesKWS1
Known GenesCYP4F12, CYP4F2, CYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987804
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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