A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545728



Internal ID18400118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1592531..1593263hg38UCSC Ensembl
Outerchr10:1592352..1593299hg38UCSC Ensembl
Innerchr10:1634726..1635458hg19UCSC Ensembl
Outerchr10:1634547..1635494hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744475
Samples
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545728
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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