A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191146



Internal ID22341895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3070366..3072593hg38UCSC Ensembl
chr6:3070600..3072827hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382228
hg192228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324848
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191146
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