A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3671154



Internal ID18969435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144080500..144199147hg38UCSC Ensembl
Innerchr7:143777593..143896240hg19UCSC Ensembl
Innerchr7:143408526..143527173hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38118648
hg19118648
hg18118648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032320
Supporting Variants
Samples
Known GenesARHGEF35, CTAGE4, OR2A12, OR2A14, OR2A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3671154
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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