A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891764



Internal ID19186160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16275195..16290783hg38UCSC Ensembl
Outerchr10:16275195..16290783hg38UCSC Ensembl
Innerchr10:16317194..16332782hg19UCSC Ensembl
Outerchr10:16317194..16332782hg19UCSC Ensembl
Innerchr10:16357200..16372788hg18UCSC Ensembl
Outerchr10:16357200..16372788hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3815589
hg1915589
hg1815589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801626
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891764
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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