A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891895



Internal ID19186291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125410838..125421233hg38UCSC Ensembl
Outerchr10:125403852..125421233hg38UCSC Ensembl
Innerchr10:127099407..127109802hg19UCSC Ensembl
Outerchr10:127092421..127109802hg19UCSC Ensembl
Innerchr10:127089397..127099792hg18UCSC Ensembl
Outerchr10:127082411..127099792hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3817382
hg1917382
hg1817382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780208, essv25779049, essv25779912, essv25786697, essv25778339, essv25779193, essv25778513, essv25801191, essv25798130
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891895
Frequency
Sample Size3017
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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