A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033274



Internal ID19122496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31111745..32127884hg38UCSC Ensembl
Innerchr9:31111743..32127882hg19UCSC Ensembl
Innerchr9:31101743..32117882hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381016140
hg191016140
hg181016140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7508n100
Supporting Variantsnssv3688843
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)nsv1033274
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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