A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036940



Internal ID19126159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55609023..55836203hg38UCSC Ensembl
Innerchr11:55376499..55603679hg19UCSC Ensembl
Innerchr11:55133075..55360255hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38227181
hg19227181
hg18227181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1193n100
Supporting Variantsnssv3505621
Samples
Known GenesOR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036940
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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