A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv669n100



Internal ID22786756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8658738..8679800hg38UCSC Ensembl
chr10:8700701..8721763hg19UCSC Ensembl
chr10:8740707..8761769hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3821063
hg1921063
hg1821063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051994, nsv1047137, nsv1052247
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)dgv669n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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