A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174450



Internal ID22332818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986772..32988358hg38UCSC Ensembl
chr1:33452373..33453959hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381587
hg191587
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n152
Supporting Variantsnssv14440916
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)nsv3174450
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