A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028443



Internal ID19117661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131018338..131430500hg38UCSC Ensembl
Innerchr4:131939493..132351655hg19UCSC Ensembl
Innerchr4:132158943..132571105hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38412163
hg19412163
hg18412163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5388n100
Supporting Variantsnssv3639456
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)nsv1028443
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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