A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1032515



Internal ID15539015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133152748..133531447hg38UCSC Ensembl
Innerchr5:132488440..132867138hg19UCSC Ensembl
Innerchr5:132516339..132895037hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38378700
hg19378699
hg18378699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599716
Supporting Variants
Samples
Known GenesFSTL4, MIR1289-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1032515
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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