A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669380



Internal ID9935485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11641743..11652540hg38UCSC Ensembl
Outerchr10:11641706..11652590hg38UCSC Ensembl
Innerchr10:11683742..11694539hg19UCSC Ensembl
Outerchr10:11683705..11694589hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810885
hg1910885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6260211
SamplesHG00653
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669380
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