A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200712



Internal ID22350122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137564224..137568965hg38UCSC Ensembl
chr9:140458676..140463417hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384742
hg194742
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381307, nssv14373121
SamplesNA19240
Known GenesDPH7
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200712
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