A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037894



Internal ID18780425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55584048..55640682hg38UCSC Ensembl
Innerchr11:55351524..55408158hg19UCSC Ensembl
Innerchr11:55108100..55164734hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3856635
hg1956635
hg1856635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1175n100
Supporting Variantsnssv3504404
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037894
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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