A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196175



Internal ID22346231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31027923..31028057hg38UCSC Ensembl
chr15:31320126..31320260hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453967
SamplesHG00733
Known GenesTRPM1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196175
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