A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508297



Internal ID18459892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55619297hg38UCSC Ensembl
Innerchr11:55361349..55386773hg19UCSC Ensembl
Innerchr11:55117925..55143349hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3825425
hg1925425
hg1825425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045911
Supporting Variants
Samples
Known GenesOR4C11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508297
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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