A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023383



Internal ID19112600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152321467..152411827hg38UCSC Ensembl
Innerchr4:153242619..153332979hg19UCSC Ensembl
Innerchr4:153462069..153552429hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3890361
hg1990361
hg1890361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5441n100
Supporting Variantsnssv3636108, nssv3636107
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)nsv1023383
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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