A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018342



Internal ID19107559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29076353..29087787hg38UCSC Ensembl
Innerchr5:29076460..29087894hg19UCSC Ensembl
Innerchr5:29112217..29123651hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3811435
hg1911435
hg1811435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635987
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)nsv1018342
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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