A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525021



Internal ID15105628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123901052..124289279hg38UCSC Ensembl
Innerchr11:123771759..124159175hg19UCSC Ensembl
Innerchr11:123276969..123664385hg18UCSC Ensembl
Innerchr11:123276969..123664385hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38388228
hg19387417
hg18387417
hg17387417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv82n21
Supporting Variantsnssv701060
Samples
Known GenesOR10G4, OR10G7, OR10G8, OR10G9, OR10S1, OR4D5, OR6T1, OR8D4, OR8G1, OR8G2, OR8G5, VWA5A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525021
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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