A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018840



Internal ID19108057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155957757..155978845hg38UCSC Ensembl
Innerchr4:156878909..156899997hg19UCSC Ensembl
Innerchr4:157098359..157119447hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3821089
hg1921089
hg1821089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5443n100
Supporting Variantsnssv3636136, nssv3636137
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)nsv1018840
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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