A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv921n152



Internal ID22816624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48675437..48675524hg38UCSC Ensembl
chr10:49883482..49883569hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3222067, nsv3213900
SamplesNA19238, NA19240, HG00513, HG00514
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)dgv921n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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