A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022791



Internal ID19112009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152337585..152376092hg38UCSC Ensembl
Innerchr4:153258737..153297244hg19UCSC Ensembl
Innerchr4:153478187..153516694hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3838508
hg1938508
hg1838508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5442n100
Supporting Variantsnssv3636123
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)nsv1022791
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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