A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv444n100



Internal ID22786531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158547194..158575633hg38UCSC Ensembl
chr1:158516984..158545423hg19UCSC Ensembl
chr1:156783608..156812047hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3828440
hg1928440
hg1828440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015106, nsv1013656
Samples
Known GenesOR6P1, OR6Y1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv444n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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