A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546257



Internal ID18400647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49069988..49070246hg38UCSC Ensembl
Outerchr10:49069932..49070296hg38UCSC Ensembl
Innerchr10:50278033..50278291hg19UCSC Ensembl
Outerchr10:50277977..50278341hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745004
Samples
Known GenesVSTM4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546257
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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