A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv683n100



Internal ID22786770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19126646..19543118hg38UCSC Ensembl
chr10:19415575..19832047hg19UCSC Ensembl
chr10:19455581..19872053hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38416473
hg19416473
hg18416473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035870, nsv1043780
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)dgv683n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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