A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735182



Internal ID18686777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96856275..98493673hg38UCSC Ensembl
Innerchr3:96575119..98212517hg19UCSC Ensembl
Innerchr3:98057809..99695207hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381637399
hg191637399
hg181637399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013060
Supporting Variants
Samples
Known GenesARL6, CRYBG3, EPHA6, GABRR3, MINA, OR5AC2, OR5H1, OR5H14, OR5H15, OR5H2, OR5H6, OR5K1, OR5K3, OR5K4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3735182
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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