A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038824



Internal ID19128043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5773466..5788096hg38UCSC Ensembl
Innerchr11:5794696..5809326hg19UCSC Ensembl
Innerchr11:5751272..5765902hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3814631
hg1914631
hg1814631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1052n100
Supporting Variantsnssv3510473
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038824
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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