A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891858



Internal ID19186254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72410114..72425880hg38UCSC Ensembl
Outerchr10:72410114..72425880hg38UCSC Ensembl
Innerchr10:74169872..74185638hg19UCSC Ensembl
Outerchr10:74169872..74185638hg19UCSC Ensembl
Innerchr10:73839878..73855644hg18UCSC Ensembl
Outerchr10:73839878..73855644hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3815767
hg1915767
hg1815767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796464, essv25796625
Samples
Known GenesMICU1, MIR1256
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891858
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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