A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079016



Internal ID18973001
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 StatusM
Merged Variants
Supporting Variantsnssv3767143
SamplesKWP1
Known GenesPLA2G4A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079016
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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