A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2947n152



Internal ID22818650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60366802..60366947hg38UCSC Ensembl
chr15:60659001..60659146hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV sva deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3276615, nsv3279262, nsv3277513
SamplesNA19240, HG00733, HG00514
Known GenesANXA2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2947n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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