A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059995



Internal ID19149214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35170778..35192851hg38UCSC Ensembl
Innerchr22:35566771..35588844hg19UCSC Ensembl
Innerchr22:33896771..33918844hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3822074
hg1922074
hg1822074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600842
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)nsv1059995
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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