A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020999



Internal ID18763533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:171858051..171976733hg38UCSC Ensembl
Innerchr5:171285055..171403737hg19UCSC Ensembl
Innerchr5:171217660..171336342hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38118683
hg19118683
hg18118683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649127
Samples
Known GenesFBXW11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020999
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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