A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028244



Internal ID19117462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159449007..159473983hg38UCSC Ensembl
Innerchr4:160370159..160395135hg19UCSC Ensembl
Innerchr4:160589609..160614585hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3824977
hg1924977
hg1824977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5447n100
Supporting Variantsnssv3636158
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)nsv1028244
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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