A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028267



Internal ID19117485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25749380..25930342hg38UCSC Ensembl
Innerchr9:25749378..25930340hg19UCSC Ensembl
Innerchr9:25739378..25920340hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38180963
hg19180963
hg18180963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755870
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)nsv1028267
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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