A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044733



Internal ID18787264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75828583..75936539hg38UCSC Ensembl
Innerchr15:76120924..76228880hg19UCSC Ensembl
Innerchr15:73907979..74015935hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38107957
hg19107957
hg18107957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717961
Samples
Known GenesFBXO22, FBXO22-AS1, UBE2Q2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044733
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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