A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545863



Internal ID18746939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7751867..7752073hg38UCSC Ensembl
Outerchr10:7751818..7752117hg38UCSC Ensembl
Innerchr10:7793830..7794036hg19UCSC Ensembl
Outerchr10:7793781..7794080hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv31e215
Supporting Variantsessv9744610
Samples
Known GenesKIN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545863
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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