A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028390



Internal ID19117608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41537118..41561271hg38UCSC Ensembl
Innerchr5:41537220..41561373hg19UCSC Ensembl
Innerchr5:41572977..41597130hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3824154
hg1924154
hg1824154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3637101
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)nsv1028390
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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