A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079015



Internal ID19323465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102426747..102504663hg38UCSC Ensembl
chr1:102892303..102970219hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3877917
hg1977917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766029
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079015
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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