A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658150



Internal ID9924255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106582761..106583142hg38UCSC Ensembl
chr1:107125383..107125764hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5476464, essv6312849, essv6080938
SamplesNA20346, NA19457, NA19328
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658150
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