A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14309893



Internal ID22204696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2940425..3030117hg38UCSC Ensembl
chr4:2942152..3031844hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3889693
hg1989693
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230727
Supporting Variants
SamplesHG00732
Known GenesGRK4, NOP14, NOP14-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14309893
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