A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061287



Internal ID19150506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47331830..47474770hg38UCSC Ensembl
Innerchr22:47727580..47870519hg19UCSC Ensembl
Innerchr22:46106244..46249183hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38142941
hg19142940
hg18142940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592270
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)nsv1061287
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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