A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891796



Internal ID18839506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43865904..43931573hg38UCSC Ensembl
Outerchr10:43865904..43931573hg38UCSC Ensembl
Innerchr10:44361352..44427021hg19UCSC Ensembl
Outerchr10:44361352..44427021hg19UCSC Ensembl
Innerchr10:43681358..43747027hg18UCSC Ensembl
Outerchr10:43681358..43747027hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3865670
hg1965670
hg1865670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780175
Samples
Known GenesLINC00840, LINC00841
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891796
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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