A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546526



Internal ID18400916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76496243..76500747hg38UCSC Ensembl
Outerchr10:76495243..76501742hg38UCSC Ensembl
Innerchr10:78256001..78260505hg19UCSC Ensembl
Outerchr10:78255001..78261500hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745273
Samples
Known GenesC10orf11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546526
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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