A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037200



Internal ID18779731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49735938..50001483hg38UCSC Ensembl
Innerchr11:49757490..50023022hg19UCSC Ensembl
Innerchr11:49714066..49979598hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38265546
hg19265533
hg18265533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1130n100
Supporting Variantsnssv3712365
Samples
Known GenesLOC440040, OR4C12, OR4C13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037200
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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