A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6675n152



Internal ID22822378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69191558..69191794hg38UCSC Ensembl
chr4:70057276..70057512hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3208617, nsv3196563
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
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)dgv6675n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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