A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038477



Internal ID19127696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109748058..109761030hg38UCSC Ensembl
Innerchr9:112510338..112523310hg19UCSC Ensembl
Innerchr9:111550159..111563131hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3812973
hg1912973
hg1812973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697655
Samples
Known GenesPALM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038477
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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