A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545721



Internal ID18400111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1409634..1410026hg38UCSC Ensembl
Outerchr10:1409535..1410088hg38UCSC Ensembl
Innerchr10:1451829..1452221hg19UCSC Ensembl
Outerchr10:1451730..1452283hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744468
Samples
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545721
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