A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013346



Internal ID18755877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:247665167..248102145hg38UCSC Ensembl
Innerchr1:247828469..248265447hg19UCSC Ensembl
Innerchr1:245895092..246332070hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38436979
hg19436979
hg18436979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv604n100
Supporting Variantsnssv3497136
Samples
Known GenesOR11L1, OR13G1, OR14A16, OR1C1, OR2AK2, OR2L13, OR2L1P, OR2L2, OR2L3, OR2L5, OR2L8, OR2T8, OR2W3, OR6F1, TRIM58
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013346
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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