A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018258



Internal ID19107475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27234186..27292711hg38UCSC Ensembl
Innerchr9:27234184..27292709hg19UCSC Ensembl
Innerchr9:27224184..27282709hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3858526
hg1958526
hg1858526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692015, nssv3692014
Samples
Known GenesEQTN, LINC00032
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018258
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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