A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546675



Internal ID18747751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91345552..91350243hg38UCSC Ensembl
Outerchr10:91344744..91350778hg38UCSC Ensembl
Innerchr10:93105309..93110000hg19UCSC Ensembl
Outerchr10:93104501..93110535hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg386035
hg196035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745422
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546675
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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