A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744711



Internal ID18718957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17053089..17059501hg38UCSC Ensembl
Outerchr10:17052002..17060001hg38UCSC Ensembl
Innerchr10:17095088..17101500hg19UCSC Ensembl
Outerchr10:17094001..17102000hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545964
Supporting Variants
Samples
Known GenesCUBN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744711
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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