A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077757



Internal ID19319953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11509269..11511468hg38UCSC Ensembl
chr18:11509268..11511467hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772281
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077757
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer