A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015259



Internal ID18757793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26347305..27643043hg38UCSC Ensembl
Innerchr9:26347303..27643041hg19UCSC Ensembl
Innerchr9:26337303..27633041hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg381295739
hg191295739
hg181295739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755877
Samples
Known GenesC9orf72, CAAP1, EQTN, IFNK, IFT74, LINC00032, LRRC19, MOB3B, PLAA, TEK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015259
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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