A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019263



Internal ID19108481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170332886..170368212hg38UCSC Ensembl
Innerchr4:171254037..171289363hg19UCSC Ensembl
Innerchr4:171490612..171525938hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3835327
hg1935327
hg1835327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5469n100
Supporting Variantsnssv3635390
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)nsv1019263
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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