A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037568



Internal ID19126787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55654851..55836092hg38UCSC Ensembl
Innerchr11:55422327..55603568hg19UCSC Ensembl
Innerchr11:55178903..55360144hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38181242
hg19181242
hg18181242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1204n100
Supporting Variantsnssv3517679, nssv3504822, nssv3513724, nssv3508348, nssv3511233, nssv3511101, nssv3519139, nssv3512856, nssv3512152
Samples
Known GenesOR4C6, 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)nsv1037568
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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