A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031444



Internal ID19120666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152337585..152385045hg38UCSC Ensembl
Innerchr4:153258737..153306197hg19UCSC Ensembl
Innerchr4:153478187..153525647hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3847461
hg1947461
hg1847461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5442n100
Supporting Variantsnssv3636124
Samples
Known GenesDEAR, FBXW7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031444
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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