A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029489



Internal ID19118708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131592892..131631063hg38UCSC Ensembl
Innerchr4:132514047..132552218hg19UCSC Ensembl
Innerchr4:132733497..132771668hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3838172
hg1938172
hg1838172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5391n100
Supporting Variantsnssv3639494
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)nsv1029489
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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