A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2989n152



Internal ID22818692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74713232..74713328hg38UCSC Ensembl
chr15:75005573..75005669hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285234, nsv3286825
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2989n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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