A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029529



Internal ID19118748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132933530..133028089hg38UCSC Ensembl
Innerchr4:133854685..133949244hg19UCSC Ensembl
Innerchr4:134074135..134168694hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3894560
hg1994560
hg1894560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5394n100
Supporting Variantsnssv3639525
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)nsv1029529
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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