A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660176



Internal ID9926281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48332683..48334345hg38UCSC Ensembl
chr4:48334700..48336362hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg381663
hg191663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5788663
SamplesNA19334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660176
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