A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546775



Internal ID18401165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103337780..103338031hg38UCSC Ensembl
Outerchr10:103337718..103338104hg38UCSC Ensembl
Innerchr10:105097537..105097788hg19UCSC Ensembl
Outerchr10:105097475..105097861hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39e215
Supporting Variantsessv9745522
Samples
Known GenesPCGF6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546775
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