A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710787



Internal ID19009068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479860..134849662hg38UCSC Ensembl
Innerchr11:134349754..134719556hg19UCSC Ensembl
Innerchr11:133854964..134224766hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38369803
hg19369803
hg18369803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040415
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710787
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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