A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655766



Internal ID18954047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29257369..29385631hg38UCSC Ensembl
Innerchr6:29225146..29353408hg19UCSC Ensembl
Innerchr6:29333125..29461387hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38128263
hg19128263
hg18128263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020683
Supporting Variants
Samples
Known GenesOR12D3, OR14J1, OR5V1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655766
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer