A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3433181



Internal ID15280137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32754397..32759495hg38UCSC Ensembl
Innerchr6:32755397..32758495hg38UCSC Ensembl
Outerchr6:32753397..32760495hg38UCSC Ensembl
chr6:32722174..32727272hg19UCSC Ensembl
Innerchr6:32723174..32726272hg19UCSC Ensembl
Outerchr6:32721174..32728272hg19UCSC Ensembl
chr6:32830152..32835250hg18UCSC Ensembl
Innerchr6:32831152..32834250hg18UCSC Ensembl
Outerchr6:32829152..32836250hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385099
hg195099
hg185099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695270
SamplesNA19239
Known GenesHLA-DQB2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3433181
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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