A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv955n152



Internal ID22816658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59697007..59697145hg38UCSC Ensembl
chr10:61456765..61456903hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV sva deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3272618, nsv3271039
SamplesHG00733, HG00514
Known GenesSLC16A9
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv955n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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