A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078297



Internal ID19324197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157378705..157488021hg38UCSC Ensembl
chr1:157348495..157457811hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38109317
hg19109317
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764979
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078297
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