A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028067



Internal ID19117285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:117005259..117092173hg38UCSC Ensembl
Innerchr5:116340955..116427869hg19UCSC Ensembl
Innerchr5:116368854..116455768hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3886915
hg1986915
hg1886915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746596
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)nsv1028067
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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