A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7615n152



Internal ID22823318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172570746..172570829hg38UCSC Ensembl
chr5:171997749..171997832hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3525076, nsv3284493
SamplesHG00732, 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)dgv7615n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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