A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv734982



Internal ID15682252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:206472931..206482290hg38UCSC Ensembl
Innerchr1:206646274..206655632hg19UCSC Ensembl
Innerchr1:204712897..204722255hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg389360
hg199359
hg189359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549068
Supporting Variants
Samples
Known GenesIKBKE, MIR6769B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv734982
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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