A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386034



Internal ID22305383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40886551..40915801hg38UCSC Ensembl
chr9:66839579..68989030hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3829251
hg192149452
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192826
Supporting Variants
SamplesNA19240
Known GenesANKRD20A1, ANKRD20A3, AQP7P1, FAM27B, FAM27E3, LOC100132352, LOC286297, LOC642236
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14386034
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