A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660786



Internal ID9926891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157156692..157175398hg38UCSC Ensembl
Outerchr3:157156655..157175448hg38UCSC Ensembl
Innerchr3:156874481..156893187hg19UCSC Ensembl
Outerchr3:156874444..156893237hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3818794
hg1918794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5966451
SamplesNA19054
Known GenesCCNL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660786
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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