A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039628



Internal ID18782159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:106180176..106649540hg38UCSC Ensembl
Innerchr13:106832525..107301888hg19UCSC Ensembl
Innerchr13:105630526..106099889hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38469365
hg19469364
hg18469364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713299
Samples
Known GenesARGLU1, EFNB2, LINC00460, LINC00551
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039628
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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