A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545925



Internal ID18747001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13216032..13216301hg38UCSC Ensembl
Outerchr10:13215973..13216372hg38UCSC Ensembl
Innerchr10:13258032..13258301hg19UCSC Ensembl
Outerchr10:13257973..13258372hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744672
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545925
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