A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183481



Internal ID22337641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77196720..77196781hg38UCSC Ensembl
chr7:76826037..76826098hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14437936
SamplesHG00514
Known GenesCCDC146, FGL2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3183481
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