A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026334



Internal ID19115552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152345024..152387222hg38UCSC Ensembl
Innerchr4:153266176..153308374hg19UCSC Ensembl
Innerchr4:153485626..153527824hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3842199
hg1942199
hg1842199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5442n100
Supporting Variantsnssv3636126
Samples
Known GenesFBXW7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026334
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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