A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019114



Internal ID19108332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130041790..130091985hg38UCSC Ensembl
Innerchr4:130962945..131013140hg19UCSC Ensembl
Innerchr4:131182395..131232590hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3850196
hg1950196
hg1850196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5387n100
Supporting Variantsnssv3639446, nssv3743098
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)nsv1019114
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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