A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv98n152



Internal ID22815801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9123310..9123394hg38UCSC Ensembl
chr1:9183369..9183453hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198234, nsv3204732
SamplesHG00512, NA19238, NA19239, NA19240, HG00513, HG00514
Known GenesGPR157
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)dgv98n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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