A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv663n100



Internal ID22786750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4244688..4269600hg38UCSC Ensembl
chr10:4286880..4311792hg19UCSC Ensembl
chr10:4276880..4301792hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3824913
hg1924913
hg1824913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052378, nsv1043787, nsv1036103
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv663n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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