A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999529



Internal ID19159066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:225868215..226092788hg38UCSC Ensembl
Innerchr2:226732931..226957504hg19UCSC Ensembl
Innerchr2:226441175..226665748hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38224574
hg19224574
hg18224574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586828
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)nsv999529
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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