A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744779



Internal ID18719025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24809188..24809456hg38UCSC Ensembl
Outerchr10:24809125..24809525hg38UCSC Ensembl
Innerchr10:25098117..25098385hg19UCSC Ensembl
Outerchr10:25098054..25098454hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744779
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