A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv232n152



Internal ID22815935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58074513..58074578hg38UCSC Ensembl
chr1:58540185..58540250hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3526883, nsv3281149
SamplesHG00512, HG00514
Known GenesDAB1
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv232n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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