A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1039n152



Internal ID22816742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104108292..104108348hg38UCSC Ensembl
chr10:105868050..105868106hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3224907, nsv3223436
SamplesHG00732, HG00733
Known Genes
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)dgv1039n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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