A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198676



Internal ID22348369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32662530..32662631hg38UCSC Ensembl
chr6:32630307..32630408hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7840n152
Supporting Variantsnssv14436953
SamplesHG00514
Known GenesHLA-DQB1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198676
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