A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698050



Internal ID15434702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55996467..56285045hg38UCSC Ensembl
Innerchr11:55763943..56052521hg19UCSC Ensembl
Innerchr11:55520519..55809097hg18UCSC Ensembl
Innerchr11:55520519..55809097hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38288579
hg19288579
hg18288579
hg17288579
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521440
Supporting Variants
Samples
Known GenesOR5AS1, OR5J2, OR5T1, OR5T2, OR5T3, OR8H2, OR8H3, OR8I2, OR8J3, OR8K5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698050
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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