A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013408



Internal ID19102626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115526309..115663615hg38UCSC Ensembl
Innerchr4:116447465..116584771hg19UCSC Ensembl
Innerchr4:116666914..116804220hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38137307
hg19137307
hg18137307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639328
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013408
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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