A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7180n152



Internal ID22822883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7262329..7267641hg38UCSC Ensembl
chr5:7262442..7267754hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385313
hg195313
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3232096, nsv3242387, nsv3243238
SamplesNA19240, HG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv7180n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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