A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737486



Internal ID19035767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48059711..48082524hg38UCSC Ensembl
Innerchr22:48455528..48478341hg19UCSC Ensembl
Innerchr22:46834192..46857005hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3822814
hg1922814
hg1822814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062943
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)nssv3737486
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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