A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7979n152



Internal ID22823682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76106270..76159073hg38UCSC Ensembl
chr6:76815987..76868790hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3852804
hg1952804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3249244, nsv3233269
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
Single strand sequencing, and assortment analysis
PlatformIllumina HiSeq
Strand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv7979n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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