A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545829



Internal ID18746905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5872908..5873933hg38UCSC Ensembl
Outerchr10:5872835..5873997hg38UCSC Ensembl
Innerchr10:5914871..5915896hg19UCSC Ensembl
Outerchr10:5914798..5915960hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381163
hg191163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744576
Samples
Known GenesANKRD16
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545829
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