A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017583



Internal ID19106800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152341706..152388386hg38UCSC Ensembl
Innerchr4:153262858..153309538hg19UCSC Ensembl
Innerchr4:153482308..153528988hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3846681
hg1946681
hg1846681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5442n100
Supporting Variantsnssv3636125
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)nsv1017583
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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