A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv878n100



Internal ID22786965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59030368..59071921hg38UCSC Ensembl
chr10:60790128..60831681hg19UCSC Ensembl
chr10:60460134..60501687hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3841554
hg1941554
hg1841554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048460, nsv1053398
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)dgv878n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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