A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659128



Internal ID9925233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:121671812..121680943hg38UCSC Ensembl
Outerchr12:121671775..121680993hg38UCSC Ensembl
Innerchr12:122109718..122118849hg19UCSC Ensembl
Outerchr12:122109681..122118899hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg389219
hg199219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv320e199
Supporting Variantsessv5429669
SamplesNA12843
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659128
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