A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8661n152



Internal ID22824364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98140129..98140197hg38UCSC Ensembl
chr7:97769441..97769509hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3284945, nsv3527832
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known GenesLMTK2
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8661n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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