A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891880



Internal ID18839590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87404437..87725505hg38UCSC Ensembl
Outerchr10:87343291..87725505hg38UCSC Ensembl
Innerchr10:89164194..89485262hg19UCSC Ensembl
Outerchr10:89103048..89485262hg19UCSC Ensembl
Innerchr10:89154174..89475242hg18UCSC Ensembl
Outerchr10:89093028..89475242hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38382215
hg19382215
hg18382215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790687, essv25791181
Samples
Known GenesLINC00864, LOC439994, MINPP1, MIR4678, NUTM2D, PAPSS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891880
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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