A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891881



Internal ID19186277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87571434..87629821hg38UCSC Ensembl
Outerchr10:87571434..87629821hg38UCSC Ensembl
Innerchr10:89331191..89389578hg19UCSC Ensembl
Outerchr10:89331191..89389578hg19UCSC Ensembl
Innerchr10:89321171..89379558hg18UCSC Ensembl
Outerchr10:89321171..89379558hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3858388
hg1958388
hg1858388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792748
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891881
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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