A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015106



Internal ID19104323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158547194..158575633hg38UCSC Ensembl
Innerchr1:158516984..158545423hg19UCSC Ensembl
Innerchr1:156783608..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 Variantsdgv444n100
Supporting Variantsnssv3498419
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)nsv1015106
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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