A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7385n152



Internal ID22823088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76336057..76336108hg38UCSC Ensembl
chr5:75631882..75631933hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3186554, nsv3186788
SamplesHG00733, 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)dgv7385n152
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