A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193536



Internal ID22343971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28578346..28579041hg38UCSC Ensembl
chr17:26905364..26906059hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14447269
SamplesHG00733
Known GenesSPAG5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193536
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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