A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381307



Internal ID22316718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137564224..137568965hg38UCSC Ensembl
chr9:140458676..140463417hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384742
hg194742
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200712
Supporting Variants
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)nssv14381307
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