A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079041



Internal ID19321934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148761315..148781687hg38UCSC Ensembl
chr3:148479102..148499474hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3820373
hg1920373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766311
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079041
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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