A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205959



Internal ID22354575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46811124..46811289hg38UCSC Ensembl
chr17:44888490..44888655hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460039
SamplesHG00733
Known GenesWNT3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205959
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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