A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545807



Internal ID18746883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4827322..4827499hg38UCSC Ensembl
Outerchr10:4827298..4827516hg38UCSC Ensembl
Innerchr10:4869514..4869691hg19UCSC Ensembl
Outerchr10:4869490..4869708hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744554
Samples
Known GenesAKR1E2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545807
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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