A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5882411



Internal ID8859814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26710086..26713224hg38UCSC Ensembl
chr10:26999015..27002153hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383139
hg193139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670796
Supporting Variants
SamplesHG00143
Known GenesPDSS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5882411
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