A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv820n100



Internal ID20152436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46428386..46470757hg38UCSC Ensembl
chr10:47078696..47121369hg19UCSC Ensembl
chr10:46498702..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3842372
hg1942674
hg1842674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049120, nsv1040445, nsv1052022
Samples
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv820n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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