A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197338



Internal ID22347234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63783072..63783834hg38UCSC Ensembl
chr10:65542832..65543594hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv961n152
Supporting Variantsnssv14390870
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)nsv3197338
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer