A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5696438



Internal ID9913341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8508518..8518164hg38UCSC Ensembl
Outerchr10:8508481..8518214hg38UCSC Ensembl
Innerchr10:8550481..8560127hg19UCSC Ensembl
Outerchr10:8550444..8560177hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389734
hg199734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666345
Supporting Variants
SamplesNA20810
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5696438
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