A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2259n106



Internal ID22796087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47894964..48516423hg38UCSC Ensembl
chr20:46523708..47132961hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38621460
hg19609254
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110861, nsv1140253
SamplesKWS2, KWS1
Known GenesLINC00494
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2259n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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