A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv928n152



Internal ID22816631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49742433..49742501hg38UCSC Ensembl
chr10:50950479..50950547hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3212335, nsv3212979
SamplesHG00733
Known GenesOGDHL
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)dgv928n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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