A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023271



Internal ID19112488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4206671..4295880hg38UCSC Ensembl
Innerchr9:4206671..4295880hg19UCSC Ensembl
Innerchr9:4196671..4285880hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3889210
hg1989210
hg1889210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758089
Samples
Known GenesGLIS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023271
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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