A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027051



Internal ID19116270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130041790..130089679hg38UCSC Ensembl
Innerchr4:130962945..131010834hg19UCSC Ensembl
Innerchr4:131182395..131230284hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3847890
hg1947890
hg1847890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5387n100
Supporting Variantsnssv3639445
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)nsv1027051
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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