A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377979



Internal ID22318371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83187290..83187386hg38UCSC Ensembl
chr15:83856042..83856138hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208092
Supporting Variants
SamplesNA19240
Known GenesHDGFRP3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377979
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