A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329679



Internal ID22206987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157147198..157147576hg38UCSC Ensembl
chr6:157468332..157468710hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209149
Supporting Variants
SamplesHG00732
Known GenesARID1B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329679
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer