A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210206



Internal ID22358161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68231415..68231632hg38UCSC Ensembl
chr17:66227556..66227773hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3613n152
Supporting Variantsnssv14431350
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210206
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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