A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv821n100



Internal ID20152437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46462388hg38UCSC Ensembl
chr10:47087031..47153919hg19UCSC Ensembl
chr10:46507037..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3866546
hg1966889
hg1866889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050898, nsv1042457
Samples
Known GenesHNRNPA1P33, LINC00842, 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)dgv821n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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