A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672657



Internal ID9938762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11352715..11356637hg38UCSC Ensembl
chr1:11412772..11416694hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383923
hg193923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5625718, essv6274262, essv5407469
SamplesHG00151, NA19082, HG00620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672657
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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