A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021409



Internal ID18763943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143875061..144176847hg38UCSC Ensembl
Innerchr7:143572154..143873940hg19UCSC Ensembl
Innerchr7:143203087..143504873hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38301787
hg19301787
hg18301787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6725n100
Supporting Variantsnssv3754832
Samples
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021409
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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