A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040886



Internal ID19130105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102484400..102534103hg38UCSC Ensembl
Innerchr9:105246682..105296385hg19UCSC Ensembl
Innerchr9:104286503..104336206hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3849704
hg1949704
hg1849704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697587
Samples
Known GenesLINC00587
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040886
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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