A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004762



Internal ID19093979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98216857..98281383hg38UCSC Ensembl
Innerchr3:97935701..98000227hg19UCSC Ensembl
Innerchr3:99418391..99482917hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3864527
hg1964527
hg1864527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4818n100
Supporting Variantsnssv3735183
Samples
Known GenesOR5H6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004762
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