A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493708



Internal ID18734663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248650779..248697630hg38UCSC Ensembl
Innerchr1:248814080..248860931hg19UCSC Ensembl
Innerchr1:246880703..246927554hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3846852
hg1946852
hg1846852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007698
Supporting Variants
Samples
Known GenesOR14I1, OR2T27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3493708
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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