A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018989



Internal ID19108206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31306001..31685361hg38UCSC Ensembl
Innerchr9:31305999..31685359hg19UCSC Ensembl
Innerchr9:31295999..31675359hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38379361
hg19379361
hg18379361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755929
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)nsv1018989
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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