A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201726



Internal ID22350987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70450328..70450379hg38UCSC Ensembl
chr17:68446469..68446520hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3622n152
Supporting Variantsnssv14407113
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201726
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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