A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767143



Internal ID18966682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186856976..186857292hg38UCSC Ensembl
chr1:186826108..186826424hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1079016
Supporting Variants
SamplesKWP1
Known GenesPLA2G4A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767143
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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