A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9577n152



Internal ID22825280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66744062..66746693hg38UCSC Ensembl
chr9:41775295..41777931hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg382632
hg192637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3207710, nsv3205878
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)dgv9577n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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