A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547031



Internal ID18748107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127739989..127740171hg38UCSC Ensembl
Outerchr10:127739947..127740209hg38UCSC Ensembl
Innerchr10:129538253..129538435hg19UCSC Ensembl
Outerchr10:129538211..129538473hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745778
Samples
Known GenesFOXI2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547031
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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