A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030328



Internal ID19119547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151870381..151954514hg38UCSC Ensembl
Innerchr4:152791533..152875666hg19UCSC Ensembl
Innerchr4:153010983..153095116hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3884134
hg1984134
hg1884134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5438n100
Supporting Variantsnssv3636094
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)nsv1030328
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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