A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025466



Internal ID19114684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19852613..20746719hg38UCSC Ensembl
Innerchr5:19852722..20746828hg19UCSC Ensembl
Innerchr5:19888479..20782585hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38894107
hg19894107
hg18894107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635916
Samples
Known GenesCDH18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025466
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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