A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv568n100



Internal ID22786655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208903927..208963474hg38UCSC Ensembl
chr1:209077272..209136819hg19UCSC Ensembl
chr1:207143895..207203442hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3859548
hg1959548
hg1859548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007896, nsv1000999, nsv1013499, nsv999126
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)dgv568n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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