A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576311



Internal ID16017034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:2419932..2611877hg38UCSC Ensembl
Innerchr18:2419931..2611876hg19UCSC Ensembl
Innerchr18:2409931..2601876hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38191946
hg19191946
hg18191946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877419
Samples
Known GenesMETTL4, NDC80
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576311
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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