A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600785



Internal ID18552380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25738059..25751045hg38UCSC Ensembl
Innerchr22:26134026..26147012hg19UCSC Ensembl
Innerchr22:24464026..24477012hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3812987
hg1912987
hg1812987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067162
Supporting Variants
Samples
Known GenesMYO18B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600785
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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