A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546052



Internal ID18400442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26710183..26712999hg38UCSC Ensembl
Outerchr10:26709780..26713276hg38UCSC Ensembl
Innerchr10:26999112..27001928hg19UCSC Ensembl
Outerchr10:26998709..27002205hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744799
Samples
Known GenesPDSS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546052
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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