A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744754



Internal ID18719000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20722350..20724582hg38UCSC Ensembl
Outerchr10:20722317..20724601hg38UCSC Ensembl
Innerchr10:21011279..21013511hg19UCSC Ensembl
Outerchr10:21011246..21013530hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744754
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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