A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670342



Internal ID9936447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5007204..5008748hg38UCSC Ensembl
Outerchr3:5007047..5008901hg38UCSC Ensembl
Innerchr3:5048889..5050433hg19UCSC Ensembl
Outerchr3:5048732..5050586hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg381855
hg191855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6203520
SamplesNA20534
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670342
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