A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019512



Internal ID19108730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22733239..22771007hg38UCSC Ensembl
Innerchr9:22733238..22771006hg19UCSC Ensembl
Innerchr9:22723238..22761006hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3837769
hg1937769
hg1837769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755838
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019512
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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