A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034864



Internal ID19124084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29069658..29087787hg38UCSC Ensembl
Innerchr5:29069765..29087894hg19UCSC Ensembl
Innerchr5:29105522..29123651hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3818130
hg1918130
hg1818130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635986
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)nsv1034864
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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