A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891773



Internal ID19186169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20202082..20304158hg38UCSC Ensembl
Outerchr10:20202082..20304158hg38UCSC Ensembl
Innerchr10:20491011..20593087hg19UCSC Ensembl
Outerchr10:20491011..20593087hg19UCSC Ensembl
Innerchr10:20531017..20633093hg18UCSC Ensembl
Outerchr10:20531017..20633093hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38102077
hg19102077
hg18102077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785899
Samples
Known GenesPLXDC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891773
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer