A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546152



Internal ID18400542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35191406..35192709hg38UCSC Ensembl
Outerchr10:35191349..35192791hg38UCSC Ensembl
Innerchr10:35480334..35481637hg19UCSC Ensembl
Outerchr10:35480277..35481719hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744899
Samples
Known GenesCREM
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546152
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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