A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016273



Internal ID19105492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20269303..20287141hg38UCSC Ensembl
Innerchr9:20269301..20287139hg19UCSC Ensembl
Innerchr9:20259301..20277139hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3817839
hg1917839
hg1817839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7472n100
Supporting Variantsnssv3690700
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)nsv1016273
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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