A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174798



Internal ID15854512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56080469..56170478hg38UCSC Ensembl
Innerchr11:55847945..55937954hg19UCSC Ensembl
Innerchr11:55604521..55694530hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3890010
hg1990010
hg1890010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555095
Supporting Variants
Samples1780862176_A
Known GenesOR8H2, OR8H3, OR8I2, OR8J3, OR8K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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