A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175357



Internal ID22333317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28346348..28346403hg38UCSC Ensembl
chr2:28569215..28569270hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464158
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)nsv3175357
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