A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013656



Internal ID19102875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158547194..158573139hg38UCSC Ensembl
Innerchr1:158516984..158542929hg19UCSC Ensembl
Innerchr1:156783608..156809553hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3825946
hg1925946
hg1825946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv444n100
Supporting Variantsnssv3704743, nssv3488789, nssv3704741, nssv3704742, nssv3704740
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)nsv1013656
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer