A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737489



Internal ID18689084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48992889..49608907hg38UCSC Ensembl
Innerchr22:49388701..50002555hg19UCSC Ensembl
Innerchr22:47774705..48388559hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38616019
hg19613855
hg18613855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062396
Supporting Variants
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)nssv3737489
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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