A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016579



Internal ID19105798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21756286..21785336hg38UCSC Ensembl
Innerchr9:21756285..21785335hg19UCSC Ensembl
Innerchr9:21746285..21775335hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3829051
hg1929051
hg1829051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690718
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)nsv1016579
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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