A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657476



Internal ID9923581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37666639..37667309hg38UCSC Ensembl
chr1:38132311..38132981hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5637895, essv6107484, essv5772479, essv5711657, essv6420942, essv5792630
SamplesNA18627, HG00419, NA19077, HG00619, NA18634, HG00476
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657476
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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