A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8784n152



Internal ID22824487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141920657..141926711hg38UCSC Ensembl
chr7:141620457..141626511hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386055
hg196055
Variant TypeCNV line1 deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3249481, nsv3248144
SamplesNA19240, 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)dgv8784n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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