A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006203



Internal ID19095421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..47091hg38UCSC Ensembl
Innerchr4:12269..47087hg19UCSC Ensembl
Innerchr4:2269..37087hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3834823
hg1934819
hg1834819
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5053n100
Supporting Variantsnssv3619227, nssv3619235, nssv3619239, nssv3619234, nssv3619238, nssv3737920, nssv3619237, nssv3619230, nssv3619228, nssv3619229, nssv3619236, nssv3619233, nssv3619232, nssv3619231
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)nsv1006203
Frequency
Sample Size11257
Observed Gain11
Observed Loss3
Observed Complex0
Frequencyn/a


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