A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5928589



Internal ID8905993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1368119..1368256hg38UCSC Ensembl
chr10:1410314..1410451hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664107
Supporting Variants
SamplesHG01107
Known GenesADARB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5928589
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