A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577622



Internal ID16018345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:72735518..72762852hg38UCSC Ensembl
Innerchr18:70402753..70430087hg19UCSC Ensembl
Innerchr18:68553733..68581067hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3827335
hg1927335
hg1827335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887305
Samples
Known GenesNETO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577622
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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