A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv819n100



Internal ID20152435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46472778hg38UCSC Ensembl
chr10:47076675..47153919hg19UCSC Ensembl
chr10:46496681..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3876936
hg1977245
hg1877245
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042166, nsv1042362, nsv1045680
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)dgv819n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss6
Observed Complex0
Frequencyn/a


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