A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033218



Internal ID19122440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1843748..1963271hg38UCSC Ensembl
Innerchr9:1843748..1963271hg19UCSC Ensembl
Innerchr9:1833748..1953271hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38119524
hg19119524
hg18119524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692356
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)nsv1033218
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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