A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192277



Internal ID22342885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68231415..68231634hg38UCSC Ensembl
chr17:66227556..66227775hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3613n152
Supporting Variantsnssv14465702, nssv14407103
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192277
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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