A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078890



Internal ID19321980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5407293..5422779hg38UCSC Ensembl
chr2:5547426..5562912hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3815487
hg1915487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766508
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078890
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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