A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3376489



Internal ID15223462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32663585..32663585hg38UCSC Ensembl
Innerchr6:32663584..32663586hg38UCSC Ensembl
Outerchr6:32663525..32663635hg38UCSC Ensembl
chr6:32631362..32631362hg19UCSC Ensembl
Innerchr6:32631361..32631363hg19UCSC Ensembl
Outerchr6:32631302..32631412hg19UCSC Ensembl
chr6:32739340..32739340hg18UCSC Ensembl
Innerchr6:32739341..32739339hg18UCSC Ensembl
Outerchr6:32739280..32739390hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3860
hg1960
hg1860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8838171
SamplesNA12878
Known GenesHLA-DQB1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3376489
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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