A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210246



Internal ID22358196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56893223..56893455hg38UCSC Ensembl
chr17:54970584..54970816hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375572
SamplesNA19240
Known GenesTRIM25
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210246
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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