A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1027n152



Internal ID22816730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99535434..99535528hg38UCSC Ensembl
chr10:101295191..101295285hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3226456, nsv3527925
SamplesHG00512, NA19238, NA19239, NA19240, HG00733
Known GenesNKX2-3
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)dgv1027n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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