A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029904



Internal ID19119123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23418574..23461154hg38UCSC Ensembl
Innerchr9:23418572..23461152hg19UCSC Ensembl
Innerchr9:23408572..23451152hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3842581
hg1942581
hg1842581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755843
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029904
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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