A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208486



Internal ID22356721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7838420..7839621hg38UCSC Ensembl
chr17:7741738..7742939hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3448n152
Supporting Variantsnssv14446519
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208486
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