A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205419



Internal ID22354110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77045365..77045452hg38UCSC Ensembl
chr18:74757321..74757408hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14446173
SamplesHG00733
Known GenesMBP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205419
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