A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033789



Internal ID19123010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22183151..22266092hg38UCSC Ensembl
Innerchr9:22183150..22266091hg19UCSC Ensembl
Innerchr9:22173150..22256091hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3882942
hg1982942
hg1882942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690722
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)nsv1033789
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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