A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7175n152



Internal ID22822878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6448622..6450258hg38UCSC Ensembl
chr5:6448735..6450371hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381637
hg191637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3186206, nsv3171469, nsv3181685
SamplesNA19240, HG00733, HG00514
Known GenesUBE2QL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv7175n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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