A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784271



Internal ID15731541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107785223..107802574hg38UCSC Ensembl
Innerchr11:107655949..107673300hg19UCSC Ensembl
Innerchr11:107161159..107178510hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3817352
hg1917352
hg1817352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556388
Supporting Variants
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784271
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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