A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780175



Internal ID18822211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43865904..43931573hg38UCSC Ensembl
Innerchr10:44361352..44427021hg19UCSC Ensembl
Innerchr10:43681358..43747027hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3865670
hg1965670
hg1865670
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891796
Supporting Variants
Samples
Known GenesLINC00840, LINC00841
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780175
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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